Amides

<p>Applications Reproduction of Sindbis virus strains sensitive and resistant to 1-adamantanecarboxamide.<br>References Erice, A., et al.: N. Engl. J. Med., 320, 289 (1989), Andronova, V.L., et al.: Bull. Exper. Bio. Med., 129, 74 (2000).<br></p>

<p>Applications 2-(Methylamino)benzamide (cas# 7505-81-9) is a useful research chemical.<br></p>

<p>Applications N,N-Diethyl-p-toluamide, is a buildig block used in the synthesis of phthalocyanines. It can also be used in preparation of new insect repellents.<br>References Liang, J., et al.: Nongyaoxue Xuebao, Vol. 16,P: 644-650 (2014);<br></p>

<p>Applications Dimethylcyanamide in the presence of tetrachlorosilane and zinc chloride is used as a promoter for one-pot, three component synthesis of a novel series of 1,3-oxazines. Being a dialkylcyanamide, it has been proved to be a more reactive substrate toward metal-mediated nucleophilic addition than alkylcyanides.<br>References Khatab, T., et al.: Indian J. Org. Chem., 11, 215 (2015); Anisimova, T., et al.: Dalton T., 42, 12460 (2013);<br></p>

<p>Applications N,N-Diethylacetoacetamide is an intermediate in the synthesis of Phosphamidon (E/Z mixture) (P353730), an organophosphate insecticide that acts as a cholinesterase inhibitor.<br>References Jacques, R., et al.: Archiv fuer Toxikologie 18: 316 (1960); Bachmann, F.: Proc. Intern. Cong. Crop. Protection, 4th Congr., 2, 1153 (1960)<br></p>

<p>Stability Hygrscopic<br>Applications N-(2,6-Dimethylphenyl)-2,2-dichloroacetamide is an intermediate used to prepare Ranolazine (R122500), an antianginal agent.<br>References Aalla, S., et al.: Org. Proc. Res. Dev.,16, 748 (2012)<br></p>

<p>Applications N-(Hydroxymethyl)acetamide (cas# 625-51-4) is used as a catalyst in the method for manufacturing sol-gel silica particles method for manufacturing coating substrate coated with silica particles.<br>References Lee, D. H., et al.: PCT Int. Appl. 23 pp. (2019)<br></p>

<p>Applications 2-aminobenzenesulfonamide (cas# 3306-62-5) is a useful research chemical.<br></p>

<p>Stability Moisture Sensitive<br>Applications 2-isothiocyanatoacetamide (cas# 145518-36-1) is a useful research chemical.<br></p>

<p>Stability Hygroscopic<br>Applications is a novel lipid-soluble, thiol-redox antioxidant and heavy metal chelator.<br></p>

<p>Applications Sulfur trioxide N,N-dimethylformamide Complex is a reagent used to prepare aminopyridines which are inhibitors of tetrameric fructose-1,6-bisphosphatase.<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 Dang, Q., et al.: J. Med. Chem., 53, 441 (2010); Hebeisen, P., et al.: Bioorg. Med. Chem. Lett., 21, 3237 (2011)<br></p>

<p>Applications 4-cyano-N,N-dimethylbenzamide (cas# 24167-50-8) is a useful research chemical.<br></p>

<p>Applications Methacrylamide (cas# 79-39-0) is a useful research chemical.<br></p>

<p>Applications 3-Amino-2-(formylamino)-3-iminopropanamide is a Temozolomide (T017775) impurity. Temozolomide acts as a imidazotetrazine alkylating agent. An antineoplastic.<br>References Newlands, E.S., et al.: Cancer Treat. Rev., 23, 35 (1997), Kim, C., et al.: J. Biol. Chem., 274, 1233 (1999), Hait, W., et al.: Cancer Res., 69, 1263 (2009),<br></p>

<p>Applications N,N'-((Ethane-1,2-diylbis(azanediyl))bis(ethane-2,1-diyl))dibenzamide is used in physical organic chemistry studies in determining proximity effects on general base catalyzed hydrolysis of amide linkage: the role of cationic surfactants, CTABr.<br>References Dash, Sarat C., Journal of Chemical Sciences (Bangalore, India), 123, 497-507, (2011)<br></p>

<p>Applications N-(2-acetyl-1-benzofuran-3-yl)-2-chloroacetamide (cas# 855715-46-7) is a useful research chemical.<br></p>

<p>Applications N-(3-Morpholinopropyl)-2-(p-tolyl)benzo[d]imidazo[2,1-b]thiazole-7-carboxamide is a useful synthetic intermediate in organic synthesis and pharmaceuticals.<br></p>

<p>Stability No Data Availabe<br>Applications 2-(4-phenyl-1,3-thiazol-2-yl)acetamide (cas# 58351-19-2) is a useful research chemical.<br></p>

<p>Applications N-(4-Hydroxymethylbenzyl)trifluoroacetamide (cas# 171723-95-8) is a compound useful in organic synthesis.<br></p>

<p>Applications 3,8-Diimino-4,7-dimethyl-2,4,7,9-tetraazadecanediimidamide is a useful research chemical.<br></p>

<p>Applications 2-Isobutyryl-N-phenyl-3-phenylacrylamide is the labeled analogue of 2-Isobutyryl-N-phenyl-3-phenylacrylamide (I781040), an intermediate for the synthesis of Atorvastatin-d5 Sodium Salt (A791753), the labeled analogue of Atorvastatin (A791750) (1,2,3). Atorvastatin is the only drug in its class specfically indicated for lowering both elevated LDL-cholesterol and triglycerides in patients with hypercholesterolemia.<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) Kearney, A.S., et al.: Pharm. Res., 10, 1461 (1993) (2) Heinonen, T.M., et al.: Clin. Ther., 18, 853 (1996) (3) Whitfield, L.R., et al.: Eur. J. Drug Metab. Pharmacokinet., 25, 97 (2000)<br></p>

<p>Applications N-(4-amino-2-chlorophenyl)-5-chloro-2-hydroxybenzamide (cas# 10558-45-9) is a useful research chemical.<br></p>

<p>N-Methoxy-N-methylacetamide is a nucleophilic amide that can be synthesized by the reaction of acetamide with methylmagnesium chloride. It has been used to synthesize an enantiopure derivative of 2-aminopropanol, which is used in the synthesis of potent antitumor agents. N-Methoxy-N-methylacetamide has shown potent anticancer activity in mice and rats. This molecule exhibits a carbonyl group that can act as an enolate, which is a reactive intermediate within chemical reactions. The nucleophilic attack on this carbonyl group leads to intramolecular hydrogen transfer, producing a more stable product.</p>

<p>Please enquire for more information about N-(5-bromo-pyridin-2-yl)-2,2-dimethyl-propionamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-(2-Chloro-4-nitrophenyl)piperazine-1-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-(Diethylamino)-N-(2,4-dimethylphenyl ) acetamide HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-Chloro-N-(2,3-dihydro-1H-inden-2-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Cyanobenzenecarboximidamide hydrochloride (NCBCH) is an intermediate for the synthesis of azomethine dyes. It can be used to produce azo dyes with a methoxy group at the 3 position and a hydrogen atom at the 4 position. NCBCH is also an excellent substrate for chemical reactions involving fragmentation, extraction, or elimination. NCBCH can be synthesized from methyl ether and benzonitrile in the presence of benzamidine. The product is then treated with methanol to give a tautomeric mixture of benzyl and methyl ether.</p>

<p>Please enquire for more information about N-Methyl-2-[[3-[(1e)-2-(2-pyridinyl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]thio]benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (NZ)-4-chloro-N-[1-[2-(4-nitrophenyl)ethyl]piperidin-2-ylidene]benzenesulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Lacosamide is an antiepileptic drug that has been shown to be bioequivalent to the reference product, Gabapentin. Lacosamide binds to voltage-gated sodium channels and is thought to have a similar clinical profile as Gabapentin. It is used in the treatment of partial seizures (with or without secondary generalization) and adjunctive therapy for generalized seizures in adults and children aged 2 years or older. Lacosamide can interact with other drugs, such as gabapentin, by increasing their serum concentrations. This interaction may lead to adverse effects such as dizziness and confusion. Lacosamide plasma concentrations are measured using LC-MS/MS methods after a two-way crossover study in healthy human volunteers. This study also showed that lacosamide is excreted unchanged in urine samples at a rate of about 50% over 24 hours, indicating that it does not undergo extensive metabolism in humans.</p>

<p>Please enquire for more information about L-Glutamic acid gamma-tert-butyl ester alpha-amide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-N,N-dipropylbenzenesulfonamide is a molecule that has been shown to be an effective antimicrobial agent against bacteria. It inhibits the growth of bacteria by inhibiting the enzyme that catalyzes the formation of acyl radicals from alkoxy radicals and ethoxycarbonyl groups. This prevents bacterial cell membrane lipid peroxidation and thus prevents bacterial growth. 4-Amino-N,N-dipropylbenzenesulfonamide also inhibits bacterial DNA synthesis by interfering with the enzymes that synthesize nucleotides and proteins. The molecule has been shown to bind to nucleophilic sites on DNA gyrase, preventing its activity, which leads to inhibition of DNA replication. 4-Amino-N,N-dipropylbenzenesulfonamide can also bind to pyrazolyl groups on carbanion molecules and form a stable carbamate group.</p>

<p>Please enquire for more information about 2-Cyano-N-cyclohexyl-N-methylacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Isonicotinamide is a coordination compound with the chemical formula (CH3)2NHCOCH2CO2N(CH3)2. It is also known as isonicotinic acid amide. Isonicotinamide has been shown to be active against resistant microorganisms, such as multidrug-resistant Mycobacterium tuberculosis and methicillin-resistant Staphylococcus aureus (MRSA). The molecular geometry of this compound is related to the intramolecular hydrogen bond that forms between the nitrogen atoms in its amide group and the oxygen atoms in malonic acid. Isonicotinamide has also been shown to have antimicrobial properties, which are likely due to its ability to chelate metal ions.</p>