3D-FA12593 - methyl-2-amino-3-nitrobenzoate
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Methyl 3-[(2-Methoxy-2-oxoethyl)amino]-4-nitrobenzoate
CAS:Methyl 3-[(2-Methoxy-2-oxoethyl)amino]-4-nitrobenzoatePurity:90%Molecular weight:268.22g/molMethyl 2-{3-[(tert-butoxycarbonyl)amino]pyrrolidin-1-yl}-5-nitrobenzoate
CAS:Methyl 2-{3-[(tert-butoxycarbonyl)amino]pyrrolidin-1-yl}-5-nitrobenzoatePurity:95%Molecular weight:365.38g/molMethyl 2-{3-[(tert-butoxycarbonyl)amino]piperidin-1-yl}-5-nitrobenzoate
CAS:Methyl 2-{3-[(tert-butoxycarbonyl)amino]piperidin-1-yl}-5-nitrobenzoate
Purity:95+%Molecular weight:379.41g/molMethyl 2-Amino-3-nitrobenzoate
CAS:Formula:C8H8N2O4Purity:>98.0%(GC)Color and Shape:Light orange to Yellow to Green powder to crystalMolecular weight:196.16Methyl 2-amino-3-nitrobenzoate
CAS:Formula:C8H8N2O4Purity:%Color and Shape:SolidMolecular weight:196.16012,4-dibromo-1,3,5-trifluorobenzene
CAS:Formula:C6HBr2F3Purity:97%Color and Shape:SolidMolecular weight:289.87534-Nitrobenzo[c][1,2,5]thiadiazole
CAS:Formula:C6H3N3O2SPurity:98%Color and Shape:SolidMolecular weight:181.1719Methyl 3-methyl-4-nitrobenzoate
CAS:Formula:C9H9NO4Purity:97%Color and Shape:SolidMolecular weight:195.1721Methyl 3-amino-4-nitrobenzoate
CAS:Formula:C8H8N2O4Purity:98%Color and Shape:SolidMolecular weight:196.1601Methyl 4-amino-3-nitrobenzoate
CAS:Formula:C8H8N2O4Purity:95%Color and Shape:SolidMolecular weight:196.1601Benzoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-3-nitro-methyl ester
CAS:Formula:C13H16N2O6Purity:98%Color and Shape:SolidMolecular weight:296.2759Benzenamine, 3-methyl-2-nitro-
CAS:Formula:C7H8N2O2Purity:98%Color and Shape:SolidMolecular weight:152.1506N-[5-(Methoxycarbonyl)-2-nitrophenyl]-DL-alanine
N-[5-(Methoxycarbonyl)-2-nitrophenyl]-DL-alaninePurity:95%Molecular weight:268.22g/molS-(5-Mercapto-2-nitrobenzoic Acid)-D-penicillamine Disulfide-d6
Controlled ProductFormula:C12D6H8N2O6S2Color and Shape:NeatMolecular weight:352.416Methyl 4-amino-3-methylbenzoate
CAS:Methyl 4-amino-3-methylbenzoate is an aromatic compound that belongs to the class of achyranthes bidentata. It can be synthesized by reacting butyryl chloride with methyl 3-nitrobenzoate. The five-membered ring in this molecule is derived from the reaction of three molecules of butyryl chloride with one molecule of methyl 3-nitrobenzoate. This reaction produces a number of possible products, including methyl 4-amino-3-methylbenzoate and 2,2,2-trichloroethyl 4-(4'-nitrophenyl)butanoate. The synthesis optimizes the reaction conditions by using a catalytic reduction technique. This reduces the amount of anilines produced and increases the yield of desired product (i.e., methyl 4-amino-3-methylbenzoate).Formula:C9H11NO2Purity:Min. 95%Molecular weight:165.19 g/molMethyl 4-amino-5-methylthiophene-3-carboxylate
CAS:Methyl 4-amino-5-methylthiophene-3-carboxylate (AMTC) is a synthetic inhibitor of the enzyme acetyl-coa carboxylase. AMTC is used as a research tool to study the role of acetyl-coa carboxylase in plants and animals. In Arabidopsis, AMTC inhibits the synthesis of fatty acids, leading to reduced seed oil content. It also inhibits transcarboxylase in wheat, which causes an accumulation of acetate. AMTC is synthesized by reacting methyl 4-nitrobenzoate with thieno[2,3,-c]pyrazole in the presence of palladium(II) chloride and potassium carbonate. The product undergoes hydrogenation to give AMTC.
Formula:C7H9NO2SPurity:Min. 95%Molecular weight:171.22 g/mol






