Alcohols

<p>4-Vinylphenol is a chemical compound that has the molecular formula CH2=CHC6H4OH. It is a hydroxyl derivative of phenol and has the chemical structure of a phenolic acid. This compound is used in the laboratory to study the effects of cationic polymerization on surface methodology and activation energies. 4-Vinylphenol inhibits Saccharomyces cerevisiae strain, which is commonly found in urine samples as well as in recombinant cells, by inhibiting cell growth and reducing ATP production. The inhibition of Saccharomyces cerevisiae strain by 4-vinylphenol can be reversed with p-hydroxybenzoic acid or cationic polymerization. The molecule also contains two nitrogen atoms that can form hydrogen bonds with other molecules, such as water molecules. It is possible that these hydrogen bonds are what allow 4-vinylphenol to inhibit Saccharomyces cerevisiae strain, although this hypothesis has</p>

<p>Phloroglucinol is a group P2 compound that has been shown to have significant cytotoxicity. It binds to the response element of phloroglucinol-induced chronic cough in vitro and in vivo, and inhibits the synthesis of DNA. Phloroglucinol is a dinucleotide phosphate that reacts with hydrogen bonding interactions. The chemical biology of phloroglucinol includes its ability to cause synchronous fluorescence at high concentrations. Phloroglucinol also possesses sodium citrate-dependent intermolecular hydrogen bonding properties.</p>

<p>3-Phenethylphenol is a hydrophobic, sterically-interacting compound that binds to molybdenum. It has been shown to inhibit the growth of fungi such as Poria and Coriolus. 3-Phenethylphenol also has functionalities such as peroxide, acetonitrile, and nature. This compound is not soluble in water and must be dissolved in solvents such as acetonitrile or polyvinyl acetate before use. 3-Phenethylphenol has been shown to have chromatographic properties, allowing it to be used as an adsorbent for the separation of organic compounds.</p>

<p>Please enquire for more information about 1-Acetyl-5-bromo-6-chloro-1H-indol-3-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromo-3-methoxybenzyl alcohol is a synthetic hydroxyphenyl compound that can be used as a coupling agent. It is prepared by the reaction of bromoacetaldehyde with 3-hydroxybenzyl alcohol in the presence of an amine base, such as pyridine. 5-Bromo-3-methoxybenzyl alcohol can also be used to synthesize pyridines and bromides.</p>

<p>Lauryl isoquinolinium bromide is a pyridinium cationic surfactant that is used as a diagnostic agent and pharmaceutical preparation. It is also used as an antimicrobial agent in liquid chromatography, which is a technique to separate chemical compounds. Lauryl isoquinolinium bromide has been shown to be effective against Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis, and Gram-negative bacteria such as Pseudomonas aeruginosa. Lauryl isoquinolinium bromide has also been shown to be effective against yeast such as Candida albicans. Lauryl isoquinolinium bromide is not effective against viruses or fungi. This agent can be used to enhance the permeability of membranes during cross-linking reactions between polymers.</p>

<p>3-Ethoxybenzyl alcohol is a lead compound that has been shown to be carcinogenic in mice. It has also been shown to have strong anti-inflammatory properties, as it inhibits the production of prostaglandins. This chemical is also able to inhibit sulfation and may be used as an analyte for high-throughput analysis in order to identify novel drugs for the treatment of asthma or other inflammatory diseases. 3-Ethoxybenzyl alcohol has a number of biological effects, including inhibition of protein synthesis and cell division, which are due to its ability to bind with sulfate ions.</p>

<p>6-Fluoro-2-iodobenzyl Alcohol is a versatile building block for the synthesis of complex compounds. It is used in research and as a reagent for the synthesis of pharmaceuticals, pesticides and other organic compounds. 6-Fluoro-2-iodobenzyl alcohol has been shown to be useful in the formation of high quality and useful intermediates, reaction components, and scaffolds. The CAS number for this chemical is 911825-94-0.</p>

<p>2-tert-Butyl-6-(5-chloro-2H-benzotriazol-2-yl)-4-methylphenol is the chemical compound with formula C12H7ClO3. It is a white solid that is soluble in water and ethanol, but not in ether or hexane. 2,6-Tertiarybutylphenol has been used as a cell nucleus marker to study locomotion of cells, as well as to analyze other samples including metal ions and water vapor. The method involves the use of a laser ablation technique, which can be used for complex sample analysis. The compound is structurally similar to 2,4,6-trimethylphenol, which has an OH group in place of the CH3 group on the tertiary butyl side chain. This difference makes it more reactive than 2,4,6-trimethylphenol because it has a higher concentration of hydroxyl groups.</p>

<p>2,3-Difluoro-4-(trifluoromethyl)phenol is a useful scaffold for the synthesis of complex compounds. The compound is a useful intermediate in the synthesis of research chemicals and speciality chemicals. It is also used as a reaction component in chemical reactions to produce fine chemicals, such as pharmaceuticals.</p>

<p>3-Bromo-5-methylphenol is an enolate that can be used to synthesize methicillin-resistant dibenzofurans. The synthesis of these compounds is a multistep process, which includes the formation of an enolate from 3-bromo-5-methylphenol and subsequent displacement with a variety of electrophiles. The use of 3-bromo-5-methylphenol as an enolate allows for high yields in the synthesis of dibenzofurans. Further, this compound has antibacterial properties and is effective against both gram positive and negative bacteria. 3-Bromo-5-methylphenol also has chloride and sulfonation properties, which have been used to make advances in the development of antibacterial agents.</p>

<p>(1R,2S)-1-Amino-2-indanol is a potential drug candidate that can be used in asymmetric synthesis. It has been shown to inhibit the flow of hydrogen bond and to form an enantiomer. The enantiomer is more active than the racemic mixture, which may be due to the higher binding affinity for the enzyme. This compound has also been shown to inhibit herpes simplex virus and HIV in vitro with a high potency. (1R,2S)-1-Amino-2-indanol is modeled using molecular dynamics simulations and quantum mechanical calculations.</p>

<p>6-Fluoro-1,2,3,4-tetrahydro-2-methylquinoline is an organocatalytic fluorine compound that has been investigated as a fluoroquinolone antibiotic. It is an enantiopure compound and has been shown to be effective in the treatment of bacterial infections. 6-Fluoro-1,2,3,4-tetrahydro-2-methylquinoline inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV. 6FLMQ is a chiral molecule with two possible configurations (R or S), which can be determined from x-ray crystallography. The S configuration is more potent than the R configuration. 6FLMQ also binds with chloride ions to form a cationic complex that can be used for antibacterial activity against Gram negative bacteria such as Escherichia coli and Pseudomonas aeruginosa.<br>6FLMQ has</p>

<p>Precusor for preparation of indinavir; a chiral ligand for asymmetric synthesis</p>

<p>4,6-Diaminoresorcinol dihydrochloride is a white solid that has viscosity and hydrochloric acid as its structural formula. It is soluble in water and reacts with proton, monosodium salt to form a precipitate. 4,6-Diaminoresorcinol dihydrochloride reacts with phosphorus pentoxide to form the sulfonation product. The thermal expansion of this material is 2.8 x 10^-5/K and it has shown chemical stability at high temperatures up to 450°C. This compound has been found to be an element analysis for chloride (Cl), hydrogen chloride (HCl) and morphology.</p>

<p>4-Hydroxy-5-iodo-3-methoxybenzyl alcohol is a polymer that has been synthesized as a model compound for lignin. It is a synthetic compound, which has not been found in nature. 4-Hydroxy-5-iodo-3-methoxybenzyl alcohol is toxic to bacteria and fungi, but not to mammalian cells. The metabolic products of this compound have not yet been identified.</p>

<p>Applications 9-(Benzyloxy)-3,7-dimethylnona-1,7-dien-4-ol is an intermediate in the synthesis of Menaquinone 6 (M218590). Menaquinones are isoprenoid quinones of the naphthalene series and belongs to the K2 Vitamin homologs. Menaquinones were originally discovered as the anti-hemorrhagic factor and now encompasses a variety of physiological processes. Menaquinone-6 were the major isoprenoid quinones found in membrane preparations of Campylobacter jejuni and Campylobacter fetus.<br>References Kiesel, B., et al.: Biodegradation, 19, 435 (2008), Suhara, Y., et al.: Bioorg. Med. Chem., 16, 3108 (2008), Gast, G., et al.: Nut., Metab., Cardiovas., Diseases, 19, 504 (2009); Carlone G.M., et al.: J. Gen. Microbiol., 129, 3385 (1983);<br></p>

<p>Applications 1,4-Cyclohexanediol is used as a reagent in the development of noviomimetics as C-terminal Hsp90 inhibitors.<br>References Anyika, M., et al.: ACS Med. Chem. Lett., 7, 67 (2016)<br></p>

<p>Applications 2,4,4-Trimethyl-2-pentanol is an intermediate formed from incubation of Sphingomonas sp. strain with xeno-estrogenic octylphenol. It was used in study comparing the relative binding affinities of low-molecular-weight proteins from humans versus male rats.<br>References Tanghe, Tom., et al.: Biodegradation, 11, 11 (2000); Borghoff, S., et al.: Toxicol. Appl. Pharm., 119, 228 (1993);<br></p>

<p>Applications Hexen-5-ol is an intermediate in he synthesis of 5-Chloro-1-hexene which is a reagent with difluoroacetic acid that results in the formation of 5-chloro-2-hexyl-2-d trifluoro-acetate and 1,4-chlorine shift.<br>References Peterson, P. E., et al.: J. Am. Chem. Soc., 86, 4503-4 (1964)<br></p>

<p>Applications 1,3-Bis(tert-Butyldimethylsiloxy)-2-propanol is an intermediate in the synthesis of 2-Linoleoyl-rac-glycerol (L467960), which is a atty acid monoglycerides in vegetable oils with medium unsaturation.<br>References Compton, D., et al.: J. Pharmacol. Exp. Ther., 277, 586 (1996), Devane, W., et al.: Science, 258, 1946 (1992),<br></p>

<p>Applications 5-(4-Hydroxypentyl)-1,3-benzenediol is an intermediate used in the synthesis of 4''-Hydroxycannabidiol (H824830), which is a metabolite of Canabidiol (C175300), a major constituents in marijuana. 4''-Hydroxycannabidiol be used to investigate canabidiol metabolism and human liver microsomes that metabolize Canabidiol into 6α-Hydroxycannabidiol.<br>References Jiang, R., et al.: Life Sci. 89, 165 (2011); Lander, N., et al.: Science 169, 611 (1970)<br></p>

<p>Applications 3-[(tert-Butyldimethylsilyl)oxy]-1-propanol (cas# 73842-99-6) is a compound useful in organic synthesis.<br></p>

<p>Applications An intermediate used in the production of various ectoparasiticides, drug metabolites and analgesic agents.<br>References Rastogi, S., et al.: J. Med. Chem., 16, 797 (1973), Maguire, J., et al.: Drug Metab. Disposition, 9, 393 (1981),<br></p>

<p>Applications Labelled form of 1-Butanol, which is used for the production of dimethylfuran for liquid fuels.<br>References Roman-Leshkov, Y. et al.: Nature, 447, 982 (2007);<br></p>

<p>Applications 2,3-Diaminophenol<br></p>

<p>Applications Intermediate for preparation of optically active theaspirane and β-Damascenone.<br>References Gertraut, S., et al.: J. Agric. Food Chem., 40, 1188 (1992), Campagnole, M., et al.: Syn. Comm., 37, 1077 (2007).<br></p>

<p>Applications A substituted alkynyl phenoxy compound as new synergists in pesticidal compositions.<br>References Hefner,T., et al.: Bioorg. Med. Chem., 10, 1731 (2002),<br></p>

<p>Applications (1R,2R)-1,2-Cyclopentanedimethanol is an intermediate in the synthesis of trans-1,2-Dimethylcyclopentane (D464925). trans-1,2-Dimethylcyclopentane was found in sedimentary rocks and was one of the hydrocarbons used to determine its maturation history.<br>References Schaefer, R.G., Littke, R.: Org. Geochem., 13, 887 (1988)<br></p>

<p>Applications 3-[[(1,1-Dimethylethyl)diphenylsilyl]oxy]-1,2-propanediol is an intermediate in the synthesis of 1,2-Dioleoyl-rac-glycerol (D482175), which is an analog of 1,3-Dioleoylglycerol (D484210) which is used in the synthesis of amphiphilic gadolinium complexes as MRI contrast agents.<br>References Accardo, A., et. al.: J. Mater. Chem. B., 1, 617 (2013)<br></p>

<p>Applications 1-Ethynylcyclohexanol is used in the preparation of 9-methyladenines used as adenosine receptor antagonists. Also used in the cycloadition of alkynes to organic azides.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Harada, H. et al.: J. Med. Chem. 44, 170 (2001); Zhang, L. et al.: J. Am. Chem. Soc., 127, 15998 (2005);<br></p>

<p>Applications 8-Bromooctan-1-ol (cas# 50816-19-8) is a useful research chemical.<br></p>

<p>Applications (3-(((2-Hydroxyethyl)(methyl)amino)methyl)phenyl)(phenyl)methanone-d3 is an intermediate in the synthesis of Nefopam-d3 (N389402), a cyclized labelled analog of orphenadrine and diphenhydramine; representative of a new class of centrally acting skeletal muscle relaxants.<br>References Bassett, et al.: Br. J. Pharmacol., 37, 69 (1969), Klohs, et al.: Arzneim.-Forsch., 22, 132 (1972), Hell, et al.: Drugs, 19, 249 (1980),<br></p>

<p>Applications 10-Amino-1-decanol (cas# 23160-46-5) is a compound useful in organic synthesis.<br>References Lee, T., et al.: J. Biol. Chem., 270, 5375 (1995),<br></p>

<p>Applications Isotope labelled Methanol (M276585), which is a common chemical reagent in organic synthesis participating in a variety of reactions. Used to prepare novel triazole-polyphenol hybrid compounds as FabG4 (Rv0242c) enzyme inhibitors for the treatment of Mycobacterium Tuberculosis (1). Also used in the synthesis of prodelphinidin B1/B2/B4 which display antitumor activities against prostate cancer cells.Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References 1. Banerjee, D. et al.: Org. Biomol. Chem. 2014 Jan 7;12(1):73-85.<br></p>

<p>Applications 6-Chloro-1-hexanol is used as a reagent in the synthesis of 3-(4-Chloro butyl)-1H-indole-5-carbonitrile; a key intermediate of the antidepressant drug Vilazodone (V265000).<br>References Anitha, N., et al.: Synthetic Commun., 44, 3563 (2014)<br></p>

<p>Applications 2,4,4-Trimethyl-1-pentanol is the principal metabolite of 2,2,4-trimethylpentane (T796535), a general solvent used in organic synthesis..<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Gaur, R. et al.: Asian J. Biochem., 10, 52 (2015);<br></p>

<p>Applications 5-Thiazolemethanol (cas# 38585-74-9) is a compound useful in organic synthesis.<br></p>

<p>Applications rac 1-O-Trimethylsilyl 3-Chloro-1,2-propanediol (cas# 1246820-26-7) is a compound useful in organic synthesis.<br></p>

<p>Applications 2,2-Diethoxyethanol is used in the synthesis of neooxazolomycin, part of the oxazolomycin family of antibiotics. Also used in the synthesis of pyrimidine based inhibitors of phosphodiesterase 7 (PDE7).<br>References Onyango, E. et al.: Angew. Chem. Int. Ed., 46, 6703 (2007); Kempson, J. et al.: Bioorg. Med. Chem. Lett., 15, 1829 (2005);<br></p>

<p>Applications 2-(4-Octylphenyl)ethanol (cas# 162358-05-6) is a compound useful in organic synthesis.<br></p>

<p>Applications (±)-3-Heptanol, is a volatile components of various plants, and can be used as flavor and fragrance ingredients. It is also used as building block used for the synthesis of various chemicals. It is used for the preparation of biologically active ester derivatives as potent inhibitors of the soluble epoxide hydrolase.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Kim, I., et al.: Bioorg. Med. Chem. Lett., 55 (18), 5889 (2012); Gibka, J., et al.: Zeszyty Naukowe - Politechnika Lodzka, 60, 65 (1998);<br></p>

<p>Applications (E)-2-Hexadecen-1-ol (cas# 26993-32-8) is a compound useful in organic synthesis.<br></p>

<p>Applications 3-Mercaptophenol is a versatile reactant used in the study of mechanism and catalysis of the native chemical ligation reaction. It was also used as a reactant in the synthesis and biological evaluation of HSP90 inhibitors based on molecular dynamic calculated conformational analysis of radicicol and its analogs.<br>References Moulin, E., et al.: J. Am. Chem. Soc., 127, 6999 (2005); Johnson, E., Kent, S.: J. Am. Chem. Soc., 128, 6640 (2006);<br></p>

<p>Applications 4-Cyanophenol is used in a study to assess chemical uptake into human stratum corneum.<br>References Stinchcomb, A.L., et. al.: Pharm. Res., 16, 1288 (1999)<br></p>

<p>Applications 10-Phthalamido-1-decanol is an intermediate used in the synthesis of 10-(t-Boc-amino)-1-decanol (B617785), which is a compound useful in organic synthesis.<br></p>

<p>Applications Hydroxyethylthio Propanol (cas# 6713-03-7) is a compound useful in organic synthesis.<br></p>

<p>Applications 3-(2-Pentyl)phenol is an intermediate in the synthesis of Bufencarb (B689385), a carbamate pesticide used mainly as an insecticide.<br>References Nesterova, T.N., et al.: J. Chem. Thermodyn., 21, 385 (1989);<br></p>

<p>Applications 3-Hexyne-2,5-diol is used in the synthesis of hyperbrancehed poly([1,2,3]-triazoles. Also used in the synthesis of pyrazoles and thiopyrazoles.<br>References Scheel, A. et al.: Macro. Rapid Comm., 25, 1175 (2004); Payne, A. et al.: Tetrahedron, 69, 9316 (2013);<br></p>

<p>Applications 3-Mercapto-1-propanol has been reported to be used as a label-free capacitive DNA detection system due to it’s terminating thiol end.<br>References Thipmanee O., et al.: Biosens Bioelectron., 38, 430-5 (2012);<br></p>

<p>Applications 2-sec-Butylphenol is a substance used in checking the effect of different enhancers on transdermal permation of insulin. It also acts as one of the substances used as models, which are helpful for aiding screening and development of androgenic compounds.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Yerramsetty, K. M., et al.: Int. J. Pharm., 398, 83 (2010); Jia, Y., et al.: isuanji Yu Yingyong Huaxue, 24, 1469 (2007)<br></p>

<p>Applications (4-(tert-Butyl)-1,2-phenylene)dimethanol is an intermediate in the synthesis of 4-tert-Butyl-1,2-bis(chloromethyl)benzene (B807070). 4-tert-Butyl-1,2-bis(chloromethyl)benzene is used as a reactant in the preparation of dihydronaphthalenes/naphthalenes via cobalt-catalyzed formal [4+2] cycloaddition of α,α'-dichloro-ortho-xylenes with alkynes.<br>References Komeyama, K., et al.: Angew. Chem. Int. Ed., 53, 11325 (2014)<br></p>

<p>Applications 2-(4-Acetoxyphenyl)ethanol is an intermediate in synthesizing Oleocanthal (O524540). It is a compound of olive oil with potential use as anti-inflammatory and chemotherapeutic agents.<br>References Scotece, M., et. al.: Drug Discovery Today, 20, 406 (2015)<br></p>

<p>Applications 3-(Dimethylamino)-1,2-propanediol is a reagent in the synthesis of 1,2-Dioleoyl-3-trimethylammonium-propane, Chloride (D484450).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications cis-2-Hexen-1-ol is used in the invention of a repellent for Oryzaephilus surinamensis.<br>References Xu, W., et al.: Faming Zhuanli Shenqing (2017), CN 107258786 A 20171020<br></p>

<p>Applications (S)-3-(Allyl(methyl)amino)-1-(thiophen-2-yl)propan-1-ol is an intermediate in the syntehsis of 4-Hydroxy Duloxetine β-D-Glucuronide Sodium Salt (H941805), which is a metabolite of Duloxetine.<br>References Lantz, R.J., et al.: Drug Dispos. Metab., 31, 1142 (2003); Detke, M., et al.: J. Clin Psy., 63, 308 (2002); Bymaster, F.P., et al.: Bioorg. Med., Chem. Lett., 13, 4477 (2003);<br></p>

<p>Applications 3-Hexyn-1-ol is an unsaturated alcohol that, when subjected to stereoselective hydrogenation, produces cis-3-Hexen-1-ol (H295005), a compound that is important in the fragrance industry. 3-Hexyn-1-ol also exhibits antifungal properties against Aspergillus oryzae, a fungus that is used to produce fermented foods and beverages in Japan.<br>References Machida, M., et al.: Nature, 438, 1157 (2005); Sachse, A., et al.: Dalt. Trans., 42, 1378 (2013); Witte, P., et al.: Stud. Surf. Sci. Catal., 175, 135 (2010)<br></p>

<p>Applications 3-(Diethylamino)-2,2-dimethylpropanol is a reactant used in the preparation of herbicides, several local anesthetics and histamine H3 receptor antagonists.<br></p>

<p>Applications 2-Phenyl-4-nitrosophenol is an intermediate in the synthesis of (E)-2-((6-Hydroxy-[1,1'-biphenyl]-3-yl)((6-hydroxy-[1,1'-biphenyl]-3-yl)imino)methyl)benzoic Acid which is an impurity of (S)-Cloperastine (C587195); a drug used in the treatment of chronic non-productive cough. Also antitussive.<br>References Aliprandi, P. et al.: Drugs Exp. Clin. Res., 30, 133 (2004); Aliprandi, P. et al.: Clin. Drug Invest. 22, 209 (2002)<br></p>

<p>Applications 1-(Benzyloxy)-3-[[bis(benzyloxy)phosphoryl]oxy]propan-2-ol is an intermediate in the synthesis of Dihydroxyacetone Phosphate Lithium Salt (D450538), which is a metabolic intermediate involved in involved in a wide variety of metabolic pathways including glycolysis and lipid biosynthesis. In plants, Dihydroxyacetone phosphate is involved with the synthesis of vitamin B6.<br>References Jun Ogawa et. al.: et al.: Bioscience, biotechnology, and biochemistry, 67(4), undefined (2003-6-6); John P Richard, Biochemistry, 51(13), undefined (2012-3-14);<br></p>

<p>Applications (S)-2-(Benzylamino)propan-1-ol is a useful research chemical for the preparation of cross-benzoin products of heteroaromatic aldehydes and amino aldehydes.<br>References Haghshenas, P., et al.: J. Org. Chem., 81, 12075-83 (2016);<br></p>

<p>Applications 1,2-Butanediol is a glycol in human serum.<br>References Imbert, L., et al.: J. Anal. Toxicol., 38, 676 (2014)<br></p>

<p>Applications 3-(3-(3-(Benzyloxy)propoxy)propoxy)propan-1-ol is an intermediate in the synthesis of 3,3'-[Oxybis(3,1-propanediyloxy)]bis[1-propanol] (O870290). 3,3'-[Oxybis(3,1-propanediyloxy)]bis[1-propanol] is derived from 3-(Benzyloxy)propyl 4-Toluenesulfonate (B288830), which is used as a reagent in the synthesis of Silodosin (S465000); an antidysuria drug. 3-(Benzyloxy)propyl 4-Toluenesulfonate is also used as a reagent in the preparation of aryloxyalkyl derivatives of adenine which have antiviral activity.<br>References Calogero, F., et al.: Eur. J. Org. Chem., 2015, 6011 (2015); Petrov, V.I., et al.: Chem. Heterocyc. Compd., 39, 1218 (2003)<br></p>

<p>Applications 2-Aminobenzyl alcohol (cas# 5344-90-1) is a useful research chemical.<br></p>

<p>Applications 1-(Phenylmethoxy)-3-(2-propen-1-yloxy)-2-propanol (cas# 83016-75-5) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-HEPTYN-1-OL (cas# 1002-36-4) is a useful research chemical.<br></p>

<p>Applications N-Benzylethanolamine is used in the synthesis of imidazoles as potent calcitonin (CGRP) antagonists. Also it aids in the preparation of benzofused hydroxamix acids, as useful fragments for the synthesis of histone deacetylase inhibitors.<br>References Tora, G. et al.: Bioorg. Med. Chem. Lett., 23, 5684 (2013); Marastoni, E. et al.: Bioorg. Med. Chem. Lett., 23, 4091 (2013);<br></p>

<p>Applications cis-3-Dodecen-1-ol is an intermediate for the synthesis of Z-3-Dodecenyl E-Crotonate, which can be used to develop insecticides and sex pheromone trap against Sweetpotato weevil.<br>References Reddy, G. V., et al.: Environ Entomol 43, 767 (2014); McQuate, G. T.: Sci Rep 4, 4499 (2014)<br></p>

<p>Stability -20°C Freezer<br>Applications Useful reagent for preparing amino acid pentachlorophenol active esters.<br>References Kovacs, J., et al.: J. Am. Chem. Soc., 89, 183 (1967)<br></p>

<p>Applications (2Z)-2-Penten-1-ol is one of the aroma volatiles in basil and thyme leaves with antioxidant activity.<br>References Lee, S., et al.: Food Chem., 91 131 (2004);<br></p>

<p>Applications cis-3-(2-Chloro-3,3,3-trifluoro-1-propen-1-yl)-2,2-dimethyl-cyclopropanemethanol is a reactant used in the preparation of pyrethroid compounds as pesticides.<br></p>

<p>2-Aminoethanethiol HCl is an organosulfur compound used in the treatment of cystinosis. Cystinosis is a rare autosomal recessive metabolic disorder that leads to the accumulation of cysteine and other amino acids in the lysosomes of cells. 2-Aminoethanethiol HCl is also used for the treatment of enteritidis, a disease caused by infection with bacteria such as Salmonella typhi, Shigella dysenteriae, or Escherichia coli. It has been shown to inhibit protein synthesis in vitro and in experimental models. The mechanism of 2-aminoethanethiol HCl's inhibition may be due to its ability to reduce mitochondrial membrane potential, thereby inhibiting ATP production and inhibiting cellular respiration.<br>2-Aminoethanethiol HCl has been found to be effective against many strains of bacteria that are resistant to standard antibiotics (e</p>

<p>1,6-Hexanediol dimethacrylate - stabilized with MEHQ is a reactive chemical that is used to generate light-sensitive particles. The light exposure of these particles causes them to react and form new bonds, which can be exploited for various applications. 1,6-Hexanediol dimethacrylate - stabilized with MEHQ has been shown to cause genotoxic effects in primary cells and cell nuclei, as well as radiation-induced DNA damage in human fibroblast cells. It has also been shown to interfere with the replication of DNA in human cancer cells. This agent is chemically similar to other known carcinogens such as allyl carbonate and benzene.</p>

<p>1,16-Hexadecanediol is a plant hormone that is structurally related to abscisic acid and gibberellins. It is found in the tissues of plants. 1,16-Hexadecanediol has been shown to have the ability to regulate plant growth and development. The diffusional properties of this molecule suggest that it may be a model system for studying other molecules with similar properties. The conformational properties of this molecule are also important because they allow for hydrogen bonding, which stabilizes the molecule and prevents it from decomposing. This property also makes 1,16-hexadecanediol an excellent candidate as a low-energy sweetener. The molecule can be seen in nmr spectra as having two peaks at different chemical shifts because it contains intramolecular hydrogen bonds. The formula weight of 1,16-hexadecanediol is 270.27 g/mol.</p>

<p>2,4-Dichlorophenol-6-sulphonyl chloride (2,4-DCP) is a molecule that has been shown to have antibacterial activity against Gram-positive and Gram-negative bacteria. It inhibits the growth of bacteria by binding to the cell wall and inhibiting enzyme activity. 2,4-DCP also has hemolytic activity in vitro. The mechanism of this effect is not well understood but may involve an interaction with membrane lipids or proteins in red blood cells. In addition, 2,4-DCP has been shown to inhibit the growth of staphylococcus and other bacterial strains in vitro. The inhibition of bacterial growth by 2,4-DCP is reversible with exposure to hydrated conditions.</p>

<p>This is a quinoline derivative that has been shown to have inotropic and cardioprotective effects. It has been shown to increase the duration of action potentials and contractions in isolated heart muscle, as well as to improve the function of the heart by reducing the rate of myocardial oxygen consumption. 6-Hydroxy-3,4-dihydro-1H-quinoline-2-one has been shown to have anti-inflammatory properties and may be useful for treating respiratory diseases such as asthma. This compound is also used as a precursor for some pharmaceutical drugs, including chloroquine, mefloquine, amodiaquine, and primaquine. The compound is metabolized into conjugates that are recycled back into the body or excreted in human urine; this process is regulated by the balance between conjugation reactions and hydrolysis reactions.</p>

<p>2-Amino-5-bromophenol is a chemical that is used as a substrate in the study of intracellular Ca2+ levels. 2-Amino-5-bromophenol can also be used to study the activity of microperoxidases, enzymes that are involved in the metabolism of hydrogen peroxide and organic hydroperoxides. 2-Amino-5-bromophenol has been shown to have anticancer activity against MCF7 cells, an estrogen receptor positive cell line. The anticancer activity may be due to the inhibition of protein synthesis by 2-amino-5-bromophenol binding to DNA. This binding prevents transcription and translation of genes that code for proteins involved in cancer cell proliferation and survival.</p>

<p>3-Chloroisoquinoline is a thiolate, which is a reactive chemical group. 3-Chloroisoquinoline has been shown to react with trifluoromethanesulfonic acid to form a compound with biological properties. The amide and palladium complexes of 3-chloroisoquinoline have been prepared in the past. Additionally, the two isomers of 3-chloroisoquinoline are known as the halides and magnetic resonance spectroscopy of this compound has been studied. Structural isomers and functional groups of 3-chloroisoquinoline have also been studied in detail. Tautomers and lactams are structural isomers of 3-chloroisoquinoline that have also been researched extensively. Finally, trifluoroacetic acid reacts with 3-chloroisoquinoline to form an ester product.</p>

<p>2-(Dimethylamino)phenol (DMP) is a neutral organic compound that is used as an analytical reagent. It reacts with hydrochloric acid to form phenols, which are then analyzed by fluorescence probe. DMP can also be used in the synthesis of aminophenols, which are used in the manufacture of dyes, pharmaceuticals, and other chemical products. It has been shown to inhibit mitochondrial functions and fatty acid synthesis. DMP binds to receptors on the surface of cells and can block the binding of drugs that target these receptors. DMP may also act as a hydrogen bond donor or acceptor depending on its environment.</p>

<p>2,4-Diaminophenoxyethanol 2HCl is a cross-linking agent that is used in the production of emulsions. It has been shown to bind to fatty acids and form an insoluble precipitate with calcium ions. This product is also effective as an adsorbent for crystal violet, which can be used for the purification of fatty acids. The adsorption kinetics of this product have been studied using a diode at different wavelengths with a wavelength of 700 nm being the most suitable for this application. 2,4-Diaminophenoxyethanol 2HCl has shown to be able to reduce weight in animals by binding water molecules and forming crystals in the body, which may contribute to its anti-obesity effects.</p>

<p>7-Methyloctanol is a polycarboxylic acid that is structurally similar to hydrochloric acid. It has been shown to have specific treatment effects on skin cells and light exposure, as well as an anti-inflammatory effect. 7-Methyloctanol is able to produce fatty acids by the hydroxylation of unsaturated alkyl chains, which are often used as plasticizers. The hydrophobic effect of 7-methyloctanol has also been shown to increase the permeability of liposomes.</p>

<p>1-Oleoyl-rac-glycerol is a lipid that has been used in experimental studies to replace the use of animal-derived lipids for pharmaceutical applications. It can be synthesized by combining oleic acid with glycerol. 1-Oleoyl-rac-glycerol is soluble in water and has been shown to have a Langmuir adsorption isotherm, which means it can be used as a monoolein substitute. The basic protein in 1-Oleoyl-rac-glycerol has been determined using XRD data and found to be chitosan polymer. The experimental model for 1-Oleoyl-rac-glycerol was tested on rats and found not to cause toxicity, making it an ideal biocompatible polymer that can be used as an alternative to chitosan polymer.</p>

<p>Linolenic acid is a polyunsaturated fatty acid that is an essential component of human nutrition. Linolenic acid has apoptosis-inducing properties and has been shown to induce the mitochondrial membrane potential in neuronal cells and induce neuronal death by decreasing the levels of pge2. Linolenic acid also participates in energy metabolism, as it can be converted into arachidonic acid, which is a precursor for prostaglandins. Linolenic acid has been shown to have physiological effects on humans, such as improving eye disorders and congestive heart failure. It does not seem to be linked with any toxicity or adverse effects.</p>

<p>4-Isopropylresorcinol or 4-Isopropylbenzene-1,3-diol belongs to the family of alkylresorcinol. It is a synthetic molecule that has been shown to reduce tumor size and inhibit cancer cell growth in vitro and in vivo. It also inhibits the expression of heat shock protein (Hsp90), which is highly expressed in most tumor cells. A study done on human lung cancer cell lines showed that 4-isopropylresorcinol inhibited the growth of xenograft tumors with no side effects, by enhancing the sensitivity of lung cancer cells to photodynamic therapy, and arrests non-small cell lung cancer cells in the G1 phase with an associated increase in apoptosis. It also induces efflux transporters in tumor cells, which leads to a time-dependent pharmacokinetics.</p>

<p>(S)-Pyroglutaminol is a chiral auxiliary that can be used to synthesize enantiopure amino acid derivatives. It is used in the synthesis of various drugs, such as antivirals and antifungals. The hydroxy group on one side of the molecule reacts with the enolate of an alpha-amino acid or a beta-keto acid to form an ester. The hydroxyl group on the other side of the molecule reacts with ethylene diamine to form an amide. Pyroglutaminol has been shown to reduce carbonyl groups in organic compounds, which may be due to its ability to act as an enantioselective catalyst for asymmetric synthesis.</p>