Methyl 4-amino-3-methylbenzoate

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CAS:18595-14-7
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Methyl 4-amino-3-methylbenzoate manufacturers

Methyl 4-amino-3-methylbenzoate Basic information
Product Name:Methyl 4-amino-3-methylbenzoate
Synonyms:4-Amino-3-methyl;Methyl 4-amino-3-methylbenzoate 98%;Methyl 4-Amion-3-Methylbenzoate;4-Amino-m-toluic acid methyl ester (COOCH3=1);Methyl 4-Aminol-3-Methylbenzoate;methyl-4-amino-3-methylbenzate;Methyl 4-amino-3-met;4-(Methoxycarbonyl)-2-methylaniline, 2-Amino-5-(methoxycarbonyl)toluene
CAS:18595-14-7
MF:C9H11NO2
MW:165.19
EINECS:
Product Categories:pharmaceutical intermediates;Phenyls & Phenyl-Het;Benzoic acid;(intermediate of telmisartan);Phenyls & Phenyl-Het;Esters;FINE Chemical & INTERMEDIATES;Amines;blocks;Chemical intermediate for Telmisartan;Aromatic Esters
Mol File:18595-14-7.mol
Methyl 4-amino-3-methylbenzoate Structure
Methyl 4-amino-3-methylbenzoate Chemical Properties
Melting point 116 °C
Boiling point 314.8±22.0 °C(Predicted)
density 1.132±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO, Methanol
pka2.32±0.10(Predicted)
form Solid
color Light Beige
CAS DataBase Reference18595-14-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-37/38-36-22
Safety Statements 26-37/39
HazardClass IRRITANT
HS Code 2922498590
MSDS Information
Methyl 4-amino-3-methylbenzoate Usage And Synthesis
Chemical PropertiesWhite to light yellow crystal powder
UsesMethyl 4-Amino-3-methylbenzoate is used in the synthesis of neuroprotective hydrazides used in the treatment of Alzheimer’s. It is also used in the research and development of diphenylamine-based retinoids.
Synthesis
Methyl 3-methyl-4-nitrobenzoate

24078-21-5

Methyl 4-amino-3-methylbenzoate

18595-14-7

The general procedure for the synthesis of methyl 4-amino-3-methylbenzoate from methyl 3-methyl-4-nitrobenzoate was as follows: methyl 3-methyl-4-nitrobenzoate (50 g, 256.2 mmol) was dissolved in methanol (1.5 L), and palladium carbon catalyst (2.5 g) was added. Hydrogen (H2) was passed into the reaction mixture at room temperature and the reaction was continuously stirred overnight. Upon completion of the reaction, the solid catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to afford the light yellow solid product methyl 4-amino-3-methylbenzoate (38 g, 90% yield). The product was analyzed by LCMS (electrospray ionization, positive ion mode) with a mass-to-charge ratio (m/z) of 166.1, corresponding to the [M + H]+ ion peak.

References[1] Tetrahedron, 2018, vol. 74, # 47, p. 6795 - 6803
[2] Journal of Heterocyclic Chemistry, 2003, vol. 40, # 6, p. 1107 - 1112
[3] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 14, p. 4582 - 4589
[4] Patent: WO2014/66795, 2014, A1. Location in patent: Paragraph 0175
[5] Zeitschrift fur Anorganische und Allgemeine Chemie, 2014, vol. 640, # 1, p. 159 - 167
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