Alcohols

<p>4-Bromo-2,6-difluorobenzyl alcohol (4BDFA) is a molecule that has been shown to be able to produce magnetic resonance images. It can be used in tumor diagnosis as well as in the imaging of tumors. 4BDFA is synthesized by coupling 2,6-difluoroaniline with bromoacetaldehyde diethyl acetal. The syntheses are carried out under phase transfer catalysis conditions and the reaction is monitored by thin layer chromatography.<br>The synthesis of 4BDFA starts with the preparation of 2,6-difluoroaniline via a Grignard reaction between aniline and magnesium metal. The Grignard reagent is then added to bromoacetaldehyde diethyl acetal in dichloromethane followed by addition of triethylamine dropwise to maintain pH neutrality. The product is then extracted from the organic solution using ethyl ether</p>

<p>(S)-(+)-1-Indanol is a substrate for the human liver alcohol dehydrogenase and can be used to study the enzyme. The molecule has two phenyl groups that are capable of forming hydrogen bonds with other molecules. The hydrogen bond is a relatively weak, noncovalent interaction between two polar molecules. It can be formed by the donation of a lone pair of electrons from one side of an oxygen atom in one molecule to a lone pair of electrons on another oxygen atom in another molecule. This type of bond is responsible for many important biological processes, including DNA replication and protein folding. The (S)-(+)-1-Indanol can also undergo carbonyl reduction, which is the conversion of an organic compound containing a carbonyl group into a corresponding hydrocarbon derivative containing hydroxyl groups. The (S)-(+)-1-Indanol contains both hydroxyl and carbonyl functionalities that make it suitable for this process. (S)-</p>

<p>Tretoquinol is a bronchodilator, which is synthesized from specific chemical reactions involving quinoline derivatives. It functions primarily as a beta-adrenergic agonist, stimulating beta-2 adrenergic receptors. This activation leads to the relaxation of bronchial smooth muscle, resulting in widened air passages and improved airflow. Tretoquinol's mechanism of action involves enhancing cyclic adenosine monophosphate (cAMP) levels, which then promotes the relaxation of the bronchial and vascular musculature.</p>

<p>(1R)-Endo-(+)-fenchyl alcohol is a chemotype of terpenes. Terpenes are hydrocarbons that are the major constituent of many essential oils and resins. The most well-known terpene is limonene, which is found in the rinds of citrus fruits. Terpenes are important for their flavors and aromas. They also have a variety of industrial uses, such as in fragrances and flavorings, paints, varnishes, and coatings. This particular chemotype has an equilibration time of 1-2 minutes at room temperature and can be prepared by evaporation or headspace techniques. (1R)-Endo-(+)-fenchyl alcohol has been detected in the aroma of grapefruit peel oil with a sensitivity of 0.5 ng/l air sample. It can be quantified using gas chromatography with flame ionization detection at 0.1 μg/l air sample or</p>

<p>3-Acetylamino-1-adamantanol is a fluorescent, non-ionic dye that is used in the preparation of coatings and optical elements. It can also be used as an oxidation catalyst for alcohols. This compound has been shown to have excellent alkaline hydrolysis and high yield in the acetonitrile process. 3-Acetylamino-1-adamantanol has been shown to react with nitro groups to form a fluorescent product. This reaction is important because it allows for the identification of explosives. 3-Acetylamino-1-adamantanol has also been found to be useful as a hologram developer or photoresist for optical discs and lenses.</p>

<p>1,2,4-Thiadiazolidine-3,5-dithione barium is a chemical building block that can be used in the synthesis of other compounds. It has been used as a reagent for research and as a speciality chemical. 1,2,4-Thiadiazolidine-3,5-dithione barium is soluble in organic solvents and is stable against heat. It can be used as an intermediate for complex compounds or as a scaffold for organic synthesis. CAS No. 82585-24-8</p>

4-Pregnen-17alpha,20alpha,21-triol-3-one (4PT) is a versatile building block that can be used in the synthesis of complex compounds. It has been used as a reagent and speciality chemical in research chemicals and as an intermediate for pharmaceuticals and other organic syntheses. 4PT also has been shown to have high quality with a reaction component and scaffold for organic synthesis.

<p>2-Chlorophenol is an organic compound that is used as a disinfectant and antiseptic. It has been shown to adsorb onto activated carbon and other organic matter in wastewater treatment facilities, where it is degraded by the intramolecular hydrogenation of 2-chlorophenol to 2-hydroxybenzoic acid. <br>This reaction can be catalyzed by sodium citrate, which acts as a proton donor. The kinetics of this transformation can be described using the pseudo-first order rate law. 2-Chlorophenol also regulates transcriptional activity through binding to DNA at specific sites. This binding can be detected using solid phase microextraction techniques on copper chloride or surfactant sodium dodecyl. The reaction mechanism for the conversion of 2-chlorophenol to 2-hydroxybenzoic acid involves intermolecular hydrogen bonding with a proton donor that leads to the oxidation of the substrate. The redox potential for this process</p>

<p>1,10-Decanediol is an organic compound that belongs to the group of glycols. It has a melting point of 117°C and a boiling point of 285°C. 1,10-Decanediol is an asymmetric molecule with two different stereoisomers: cis-1,10-decanediol and trans-1,10-decanediol. The melting point for cis-1,10-decanediol is higher than that for trans-1,10-decanediol. This indicates that the cis form is more stable at room temperature than the trans form. 1,10-Decanediol can be used in the synthesis of fatty acids and dna duplexes. It has also been shown to inhibit the replication of HIV by binding to its reverse transcriptase enzyme and preventing it from functioning properly.</p>

<p>2-(2,5-Dichlorophenyl)ethanol (2,5-DCPE) is an organic chemical that is used as a building block for the synthesis of fine chemicals and pharmaceuticals. 2,5-DCPE can be used as a reactant in synthesizing more complex compounds. It reacts with many different functional groups to form covalent bonds. The compound has been shown to have high quality and has been characterized by nuclear magnetic resonance spectroscopy and mass spectroscopy.</p>

<p>N-Methyl-5-tetrazolethiol is a vitamin B6 (pyridoxine) analog that inhibits bacterial growth by competitively inhibiting enzymes involved in the synthesis of folate. It has been shown to be toxic for animals and humans at high doses, but the toxicity of this compound has not been studied extensively. N-Methyl-5-tetrazolethiol has been shown to inhibit the activity of enzymes such as methionine synthase, cytochrome C reductase, and nitroreductase in vitro. This drug is used as a treatment for infectious diseases such as malaria and toxoplasmosis. The mechanism of action of N-methyl tetrazolethiol is not known, but it is believed to be related to its ability to inhibit enzyme activity.</p>

4-Methylresorcinol is a phenolic compound that has been shown to have a broad spectrum of antimicrobial activity. It is an inhibitor of 3-hydroxybenzoic acid, a key metabolic intermediate in the biosynthesis of aromatic amino acids and lignin. 4-Methylresorcinol inhibits the enzyme tyrosine ammonia lyase, which converts tyrosine to 3-hydroxybenzoic acid. The synthetic nature of 4-methylresorcinol makes it an attractive candidate for use as an antifungal agent, since it does not produce any byproducts in the human body. 4-Methylresorcinol also has antifungal activity against other organisms such as Candida albicans, Aspergillus niger, and Trichoderma viride.

2-Chloro-1-methylquinolinium tetrafluoroborate (2CQBF) is a synthetic compound that inhibits protein synthesis. It has been used as an analytical reagent for the determination of proteins, including those in urine samples. 2CQBF has been shown to be effective in the treatment of cancer and other diseases, such as lupus erythematosus, arthritis, and psoriasis.

<p>Allopurinol is a drug that is used in the treatment of gout and other disorders caused by excessive production of uric acid. It functions as an inhibitor of xanthine oxidase, which is the enzyme responsible for converting hypoxanthine to xanthine, and xanthine to uric acid. Allopurinol blocks the conversion of these compounds, thereby reducing the formation of uric acid. Allopurinol has been shown to be effective for treating inflammatory bowel disease such as ulcerative colitis and Crohn's disease. This drug also inhibits nuclear DNA synthesis, antioxidant vitamins (e.g., vitamin E), and brain functions. Allopurinol has been shown to be effective in protecting neurons against oxidative injury that may lead to neurodegenerative diseases such as Parkinson's disease.</p>

<p>2,4,6-Tribromo-3-methoxyphenol is a high quality reagent that is used as an intermediate in the production of many fine chemicals. It is also a useful building block for the synthesis of speciality chemicals and research chemicals. This chemical can be used as a versatile building block for reactions with other compounds. 2,4,6-Tribromo-3-methoxyphenol has CAS number 24967-79-1 and can be found at Chemical &amp; Laboratory Equipment.</p>

<p>Iodoquinol is a quinoline derivative that has been shown to have antifungal properties in vitro. It is used to treat bowel disease and infectious diseases, such as malaria and tuberculosis. Iodoquinol has also been shown to reduce the incidence of autoimmune diseases by inhibiting the production of pro-inflammatory cytokines. The mechanism of action for this drug is not well understood, but it is believed that it reacts with DNA and may inhibit the synthesis of proteins. It has also been shown to cause genotoxic effects in a model system by binding covalently to DNA, as well as benzalkonium chloride</p>

<p>Fmoc-L-threoninol is a conjugate of L-threoninol with a protecting group, Fmoc. It is synthesized by the solid-phase method on an activated resin and then cleaved from the resin to give the desired product. The linker used in this synthesis is succinic acid diacetate. This compound has been shown to have anti-inflammatory effects in human serum, which may be due to its ability to inhibit prostaglandin synthesis.</p>

2-Nitroethanol is a chemical compound that is used as an antioxidant, antimicrobial preservative, and flavoring agent in foods. It can be synthesized in an asymmetric synthesis reaction, which involves the addition of a nitro group to one of the two carbons in ethylene glycol. The toxicity profile of 2-nitroethanol has not been extensively studied, but it appears to have low toxicity based on animal studies. A number of inhibitory compounds have been identified for 2-nitroethanol, including benzalkonium chloride and propionate. The inhibitory effects of 2-nitroethanol are concentration dependent and may be due to hydrogen bonding with proteins or intramolecular hydrogen transfer reactions with other molecules. Inhibition of viral replication by 2-nitroethanol has been observed in influenza virus and human immunodeficiency virus (HIV) studies. This inhibition may be due to alterations in fatty acid metabolism or changes in the

<p>Intermediate in the synthesis of vildagliptin</p>

4-Amino-2-chlorophenol is an aminophenol that is used in the production of acetate, which is used in the manufacture of acetic acid. It is also used as a building block for organic synthesis. 4-Amino-2-chlorophenol reacts with acetyl chloride to form chloracetyl chloride, which can then be reacted with piperonyl butoxide to form 2-(4'-aminophenyl)-4,6-dichloropyridine. This reaction is catalyzed by hydrogen chloride and hydrogen bond formation with urea nitrogen. 4-Amino-2-chlorophenol has been shown to have long-term toxicity in animal studies and may be toxic when inhaled or ingested.

DL-Homocysteine thiolactone hydrochloride is a compound that has been found in human serum and urine. It is used to measure the concentration of homocysteine in the blood, which may be an indicator of coronary heart disease. DL-Homocysteine thiolactone hydrochloride is used to synthesize the amino acid cysteine, which is vital for cell growth and protein synthesis. DL-Homocysteine thiolactone hydrochloride also has optical properties that make it suitable as a photochromic material. The compound has been shown to be a hydrogen bond donor, which makes it useful for stabilizing proteins in mammalian cells.

<p>5,7-Dibromo-8-hydroxyquinoline is a cytotoxic agent that has been shown to inhibit the growth of xenograft tumor cells. It was found to be effective in inhibiting the mitochondrial membrane potential and decrease the rate of cell proliferation. 5,7-Dibromo-8-hydroxyquinoline also showed significant cytotoxicity against carcinoma cell lines, with no effect on normal human fibroblast cells. The drug is an organophosphate compound that inhibits fatty acid synthesis by binding to an enzyme involved in fatty acid biosynthesis. This inhibition causes diarrhoea and sodium salt loss. 5,7-Dibromo-8-hydroxyquinoline can be extracted from hydrochloric acid through a solvent extraction process.</p>

<p>1,1,1-Trifluoro-2-propanol (TFHP) is a molecule that contains three hydrogen atoms and two fluorine atoms. It has a frequency shift of 0.00116 cm−1 in the infrared spectrum due to the conformational properties of its hydroxyl group, which causes the OH stretching vibration to be shifted. TFHP is a weak acid that reacts with sodium trifluoroacetate to form trifluoroacetic acid and hydroxyl ions. TFHP has been shown to have biological properties in bacteria, such as inhibiting bacterial growth and suppressing protein synthesis. The molecular structure of TFHP is made up of a hydrogen atom on each nitrogen atom, which is then bonded to an intramolecular hydrogen bond and an intermolecular hydrogen bond with other TFHP molecules. The deuterium isotope can also be found in this compound, which will cause a shift in IR frequency from 0.00116 cm</p>

<p>Triphenylphosphonium is a reactive phosphonium salt that is used as an intermediate in the synthesis of 1,2,4-butanetriol. The synthesis of the triphenylphosphonium salt from the sodium salt of butyric acid and ferrocene is shown in this scheme. This synthetic route provides for planar chirality and an asymmetric synthesis. The byproduct, butyric acid, can be converted to its conjugate base with ammonium hydroxide or sodium hydroxide to provide cholic acid. Cholic acid is a hepatoprotective agent that has been used in the treatment of liver disease.</p>

<p>Biotinyl-6-aminoquinoline is a synthetic chemical that has been shown to inhibit the growth of cancer cells in laboratory mice. It was synthesized to be a substrate for the enzyme quinolinate synthase, which is involved in the synthesis of nicotinic acid. Biotinyl-6-aminoquinoline is an analytical method that has been used in urinary samples from patients with bladder cancer as well as healthy individuals. The sequences of each individual were determined and analyzed using an algorithm that performs logistic regression, which can predict whether or not the patient has bladder cancer.</p>

Pabulenol is an innovative biopolymer, which is synthesized from renewable plant-based resources through advanced biotechnological methods involving enzymatic polymerization. With its unique molecular structure, Pabulenol exhibits specific mode of action by facilitating biodegradation under ambient conditions, catalyzed by naturally occurring microbes. The polymer’s intrinsic ability to break down into non-toxic byproducts makes it an exceptional choice for sustainable environmental applications.

<p>Deoxypyridinoline chloride 3HCl is a fine chemical that is used as a building block in the synthesis of organic compounds. Deoxypyridinoline chloride 3HCl can be used as a reagent and speciality chemical in research laboratories, as well as in the manufacture of pharmaceuticals and other organic molecules. Deoxypyridinoline chloride 3HCl is also versatile, serving as an intermediate to produce other chemicals, or as a reaction component to produce complex products with specialized properties. The compound has been registered by the Chemical Abstracts Service (CAS) under CAS No. 204074-56-6.</p>

4-Butoxy-1-butanol is a solvent that has been shown to be safe for use in humans. It is used to modify the chemical structure of d-glycero-d-galacto-heptose and can be used as a solvent. 4-Butoxy-1-butanol was found to be safe for primary cells and was able to normalize their metabolism and growth rate. This compound has also been shown to have diagnostic properties based on its ability to inhibit the production of camaldulensis leaves, which are known to produce naphthalene. The mechanism by which this compound inhibits camaldulensis leaf production is unknown, but it may involve an acceptor molecule or biochemical reactions.

<p>2-(Aminooxy)ethanol is an organic compound that has the chemical formula CH3NOCH2CH2OH. It belongs to the group of cyclic ketones and is a colorless liquid with a boiling point of 78°C. This substance can be produced by dehydrogenation of ethylene oxide or by reaction of formamide with sodium hydroxide and hydrochloric acid. The product can also be prepared from 2-hydroxyethanol, which reacts with ethylene in presence of HCl. The reaction time for this process is around 1 hour at room temperature. The chemical formula for 2-(Aminooxy)ethanol is C4H11NO2O.</p>

<p>8-Fluoroquinoline is a quinoline derivative that has been shown to have in vitro anticancer activity against colon adenocarcinoma cells. It is a chiral molecule that can exist as two stereoisomers, (R)-8-fluoroquinoline and (S)-8-fluoroquinoline. These isomers may have different interactions with the tumorigenic cells, but both of them have anticancer activity. 8-Fluoroquinoline also interacts with cytochrome P450 enzymes, enhancing their ability to metabolize carcinogens.</p>

N-[2-(p-Cinnamylamino)ethyl]-5-isoquinolone sulfonamide is a high quality chemical that can be used as a reagent, complex compound, and useful intermediate. N-[2-(p-Cinnamylamino)ethyl]-5-isoquinolone sulfonamide is a fine chemical that is useful in the production of speciality chemicals. It can be used as a versatile building block and reaction component to produce various compounds.

<p>Bis(8-quinolinolato)zinc (II) is a molecule that contains carboxylate groups. It has been shown to be processable and can be used in fabrication processes. Bis(8-quinolinolato)zinc (II) also exhibits optical properties. The metal ion in the molecule is able to form complexes with other metals, which may affect transport properties, ionization mass and morphology of the compound. It can also be used for magnetic resonance spectroscopy studies, as well as plasma mass spectrometry.</p>

(S)-Glycerol 1-benzyl ether is a chiral, synthesised antidepressant drug that has shown to be effective in the treatment of depression. It binds to α-adrenergic receptors and blocks the binding of norepinephrine and epinephrine, preventing the production of stress hormones. (S)-Glycerol 1-benzyl ether is also used as a reagent for the synthesis of doxazosin and d-mannitol.

3-Chloro-4-(trifluoromethyl)benzyl alcohol is a versatile building block for synthesis of various chemical compounds. It is used as a reagent, reaction component, or building block in organic synthesis. It is also useful as a speciality chemical or research chemical. CAS No. 65735-71-9

<p>The fluoroquinolone 5-Fluoro-2-methylphenol (5FM) is an inhibitor of angiotensin, an enzyme that is involved in the regulation of blood pressure and fluid balance. The structure of this compound was optimized to make it more potent and selective for angiotensin, while minimizing its adverse effects. This optimization was achieved using high throughput screening and x-ray crystallography. The fluorine atom in 5FM binds to aspartyl protease, which prevents the protease from breaking down proteins into smaller amino acid chains. This binding also inhibits the activity of other enzymes that are involved in protein synthesis, such as aspartyl proteases and salicylic acid esterases. 5FM has been shown to inhibit the growth of bacteria such as Staphylococcus aureus at concentrations that are not toxic to mammalian cells.</p>

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

<p>3,5-Dibenzyloxybenzyl alcohol is a flavonoid that is used for the treatment of cancer. The compound inhibits the activity of cyclooxygenase-2 (COX-2) and has been shown to inhibit the production of prostaglandin E2, which is associated with inflammation. 3,5-Dibenzyloxybenzyl alcohol also inhibits metathesis reactions in an equilibration process that can be catalyzed by palladium or platinum. It has been found to have anti-inflammatory properties due to its inhibition of COX-2 and its ability to induce apoptosis in tumor cells. 3,5-Dibenzyloxybenzyl alcohol also has anti-cancerous properties, which may be due to its ability to inhibit cell proliferation through alkylation and spiroketal conjugation reactions. This compound also binds to tannins and fatty acids as well as monomers in a reversible manner</p>

Polidocanol is a non-ionic surfactant that is used in the preparation of biological samples for microscopy. It can be used to separate cells from a homogenized tissue sample, and to extract lipids from cell membranes. Polidocanol has been shown to have anti-cancer activity against a number of different types of cancer including colon, breast, lung, prostate, and leukemia. This compound was found to inhibit tumor growth by interfering with the synthesis of fatty acids and proteins. Polidocanol was found to be effective in preventing the formation of multicellular clusters of Candida glabrata cells on agar plates. This may be due to its ability to disrupt the surface tension between cells and water molecules, which prevents their attachment to each other. Polidocanol also has hemolytic activity that can be seen when it is added to red blood cells in solution.

<p>1-(4-Methylphenyl)ethanol is a colorless liquid that has a low energy and functional groups. It can be used as a reaction product in vitro assays and rhizosphere. 1-(4-Methylphenyl)ethanol reacts quickly with high salt, phosphatase, and silicon. The rate of the reaction increases with an increase in temperature. 1-(4-Methylphenyl)ethanol is also used for cationic polymerization, which is used to detect cirrhosis, high salt, phosphatase, and silicon by optical properties.</p>

(6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol hydrochloride is a reagent that can be used as an intermediate for the synthesis of many complex compounds. It is a useful building block for the synthesis of pharmaceuticals with speciality chemicals and research chemicals. This compound has been shown to be a versatile building block in the synthesis of natural products, pharmaceuticals and other organic molecules. (6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol hydrochloride is also a reaction component that can be used to synthesize many chemical substances with different functional groups.

<p>3-(Aminomethyl)adamantan-1-ol HCl is a chemical substance that can be used as a reaction component, reagent, and useful scaffold in the synthesis of pharmaceuticals. It is also a speciality chemical with versatile building block and useful intermediate properties. 3-(Aminomethyl)adamantan-1-ol HCl has been shown to be an effective building block for complex compounds, such as those used in the synthesis of anti-inflammatory drugs.</p>

<p>1,4-Dibromo-2,3-butandiol is a halogenated butandiol.</p>

<p>4-Methoxy propranolol is an intermediate in the synthesis of propranolol, a beta blocker.</p>

<p>Xanthinol nicotinate is a fat-soluble compound that is found in the form of nicotinic acid. It has been shown to decrease inflammation, inhibit tumor growth and improve blood flow. Xanthinol nicotinate has been shown to be effective for the treatment of chronic pulmonary disease, cranial cavity disease, maternal blood clotting disorders, congestive heart failure, cancer, and tissue culture. This drug has also been shown to regulate transcriptional activity and coordinate complex formation. The use of this drug has also been shown to be beneficial for women with diabetes mellitus or pancreatitis.</p>

Acetylcorynoline is a known metabolite of protopine, which is an alkaloid found in plants. Acetylcorynoline has been shown to have p450 activity, and can be used as a model for the study of this enzyme. Acetylcorynoline is also involved in energy metabolism and its concentration in urine samples may be indicative of chronic bronchitis. Acetylcorynoline can be prepared using preparative high performance liquid chromatography (HPLC) methods, and has pharmacokinetic properties that are similar to other metabolites of protopine.

2-Bromo-5-(trifluoromethyl)benzyl alcohol is a fine chemical that is used as an intermediate in the synthesis of other chemicals. It can be used to synthesize novel organic compounds, such as pharmaceuticals and pesticides. This chemical has been shown to react with various other organic compounds, including amines, thiols, and carboxylic acids. 2-Bromo-5-(trifluoromethyl)benzyl alcohol is also known for its ability to form complexes with metals.

<p>The asymmetric synthesis of 4-chlorodiphenylcarbinol is an efficient method that uses a simple, inexpensive, and environmentally friendly reagent. The reaction proceeds in the presence of hydrochloric acid and sodium hydroxide solution. The reaction mechanism is the same as for the preparation of other chiral alcohols. The stereoselective preparation method is based on the use of glycol esters or trifluoroacetic acid to produce enantiomerically pure 4-chlorodiphenylcarbinol, which can be used as a precursor for pharmaceuticals, pesticides, and dyes.</p>

<p>2,5-Dimethyl-2,5-hexanediol is an organic compound that consists of a linear polymer. It can be found in natural gas and crude oil as well as in the atmosphere. 2,5-Dimethyl-2,5-hexanediol is used to make polyester resins and plasticizers. It can also be used as a solvent or a reactant in organic syntheses such as alkylation reactions. 2,5-Dimethyl-2,5-hexanediol has intramolecular hydrogen bonds which help it to have high transport properties. The molecule of 2,5-dimethyl-2,5 hexanediol consist of two ethane groups linked by a linear chain consisting of alternating methyl and hydroxyl groups. The molecular formula for this compound is CH(CH)CHOHCHOHCH(CH)OH. This compound has two sets of electron orbitals that are parallel to each other with one set being perpendicular to</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>4,5-Bis(2-cyanoethylthio)-1,3-dithiole-2-thione is a fluorescent compound that exists in two orientations, cis and trans. It has been used as a linker for the construction of new compounds with interesting properties. 4,5-Bis(2-cyanoethylthio)-1,3-dithiole-2-thione has been shown to be an effective ligand for palladium cross coupling reactions. This compound can also be used in supramolecular chemistry due to its ability to fluoresce brightly.</p>