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METHYL 5-AMINO-2-METHYL-3-NITROBENZOATE is an organic compound that serves as an intermediate in the synthesis of various pharmaceutical compounds.
Used in Pharmaceutical Industry:
METHYL 5-AMINO-2-METHYL-3-NITROBENZOATE is used as an intermediate in the synthesis of 3-Amino-5-nitro-o-toluamide (A105200), a metabolite of the veterinary drug zoalene. This intermediate plays a crucial role in the production of drugs for veterinary use, contributing to the development of medications that improve animal health and well-being.

88132-48-3

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88132-48-3 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 27, p. 386, 1984 DOI: 10.1021/jm00369a026

Check Digit Verification of cas no

The CAS Registry Mumber 88132-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88132-48:
(7*8)+(6*8)+(5*1)+(4*3)+(3*2)+(2*4)+(1*8)=143
143 % 10 = 3
So 88132-48-3 is a valid CAS Registry Number.

88132-48-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-amino-2-methyl-3-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 5-amino-2-methyl-3-nitro-benzoic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88132-48-3 SDS

88132-48-3Relevant academic research and scientific papers

Nucleophilic substitution of the acetoxy group in 3- methylbenzoylaminomethyl acetate

Labanauskas,Mazeikaite,Striela,Gedrimaite,Urbelis,Zilinskas

experimental part, p. 1672 - 1676 (2012/09/05)

Replacement of the acetoxy group in 3-methylbenzoylaminomethyl acetate with N- and S-nucleophiles generated from amines and thio compounds using sodium hydride gives the corresponding N-aminomethyl- and N-thiomethylbenzamides.

6-Hydroxy-4-[2-(di-n-propylamino)ethyl]indole: Synthesis and dopaminergic actions

Cannon,Lee,Ilhan,Koons,Long

, p. 386 - 389 (2007/10/02)

The title compound was proposed to be a biologically active metabolite of a dopaminergic agent, 4-[2-(di-n-propylamino)ethyl]indole. This proposed metabolite was synthesized by a multistep sequence beginning with methyl 3,5-dinitro o-toluate, and involvin

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