58605-12-2 (2,4-二硝基苯乙酸甲酯,Methyl 2,4-Dinitrophenylacetate)

2,4-二硝基苯乙酸甲酯;2,4-二硝基苯基乙酸甲酯;

Methyl 2-(2,4-dinitrophenyl)acetate;Aceticacid, (2,4-dinitrophenyl)-, methyl ester (6CI);(2,4-Dinitrophenyl)acetic acidmethyl ester;Methyl (2,4-dinitrophenyl)acetate;NSC 143979;Benzeneacetic acid,2,4-dinitro-, methyl ester;METHYL 2 4-DINITROPHENYLACETATE;(2,4-dinitrophenyl)-acetic acid methyl ester;2.4-Dinitro-phenylessigsaeure-methylester;BEN173;methyl 2,4-dinitrobenzeneacetate;Methyl 2,4-dinitrophenyl acetate;MFCD00047704;methyl2-(2,4-dinitrophenyl)acetate;FT-0640543;G10106;Methyl 2,4-dinitrophenylacetate;BB 0243945;FH-0034;2,4-dinitrophenylacetic acid methyl ester;NSC-143979;SCHEMBL2133926;2,4-dinitrophenyl-acetic acid methyl ester;AKOS003375803;NSC143979;CS-0130247;(2,4-Dinitro-phenyl)-acetic acid methyl ester;AMY25133;58605-12-2;DTXSID40301523;DB-050291;ALBB-023360;Benzeneacetic acid, 2,4-dinitro-, methyl ester;

MFCD00047704

HTANURMJHZJJSO-UHFFFAOYSA-N

1S/C9H8N2O6/c1-17-9(12)4-6-2-3-7(10(13)14)5-8(6)11(15)16/h2-3,5H,4H2,1H3

O(C)C(CC1C=CC(=CC=1[N+](=O)[O-])[N+](=O)[O-])=O

医药中间体。;

2,4-二硝基苯乙酸与甲醇酯化而得。将216g2,4-二硝基苯乙酸溶于1100ml无水甲醇中，加热至沸，缓缓通入干燥的氯化氢气体。冷却，析出2,4-二硝基苯乙酸甲酯。过滤，干燥，得产品192g，收率80%。