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Sku CI27872_25_G
Chem Impex
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Product Information

Product Name
2-Methyl-3-nitrobenzoic acid methyl ester
Brand Name
Chem Impex
Product Number
27872
CAS
59382-59-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
601165
IUPAC Name
methyl 2-methyl-3-nitrobenzoate
InChI Key
CRZGFIMLHZTLGT-UHFFFAOYSA-N
SMILES
CC1=C(C=CC=C1N+(=O)O-)C(=O)OC

Description

2-Methyl-3-nitrobenzoic acid methyl ester is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly in creating anti-inflammatory and analgesic drugs.

Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and pesticides, enhancing crop protection and yield.

Polymer Chemistry: The compound acts as a building block in the development of specialty polymers, contributing to materials with enhanced properties such as durability and resistance to degradation.

Analytical Chemistry: It is employed as a standard in chromatographic techniques, aiding in the accurate analysis of complex mixtures in research laboratories.

Environmental Studies: The compound is utilized in studies assessing the environmental impact of nitro compounds, helping researchers understand their behavior and degradation in ecosystems.

References Data Source From Pubchem

Experimental design optimization for the synthesis of lenalidomide nitro precursor

Publication Name: Research on Chemical Intermediates
Publication Date: 2022-11-17
DOI: 10.1007/s11164-022-04869-5

Fundamental Studies of New Ionization Technologies and Insights from IMS-MS

Publication Name: Journal of The American Society for Mass Spectrometry
Publication Date: 2019-05-06
DOI: 10.1007/s13361-019-02194-7

Scalable and green process for the synthesis of anticancer drug lenalidomide

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2015-02
DOI: 10.1007/s10593-015-1670-0

From 2-(o-Nitroaryl)enamines; Leimgruber–Batcho Synthesis

Publication Name: Science of Synthesis
Publication Date: 2010

Lenalidomide

Publication Name: Pharmaceutical Substances
Publication Date: 2006