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Product Information

Product Name
4-Methyl-3-nitrobenzoic acid
Brand Name
Chem Impex
Product Number
22019
CAS
96-98-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7319
IUPAC Name
4-methyl-3-nitrobenzoic acid
InChI Key
BBEWSMNRCUXQRF-UHFFFAOYSA-N
SMILES
CC1=C(C=C(C=C1)C(=O)O)N+(=O)O-

Application

4-Methyl-3-nitrobenzoic acid 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.

Dyes and Pigments: It is used in the production of dyes and pigments, providing vibrant colors for textiles and plastics, which are essential in the fashion and manufacturing industries.

Polymer Chemistry: The compound is utilized in the development of specialty polymers, enhancing properties such as thermal stability and chemical resistance, which are crucial for automotive and aerospace applications.

Analytical Chemistry: It acts as a reagent in various analytical techniques, aiding in the detection and quantification of other chemical substances, which is vital for quality control in laboratories.

Research in Environmental Science: The compound is studied for its potential impact on environmental health, helping researchers understand the degradation processes of nitro compounds in ecosystems.

References

Phytochemistry, pharmacological applications, and therapeutic effects of green synthesized nanomaterials using Cichorium species—a comprehensive review

Publication Name: Naunyn-Schmiedeberg's Archives of Pharmacology
Publication Date: 2024-06-20
DOI: 10.1007/s00210-024-03221-5

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells

Publication Name: Biochemical and Biophysical Research Communications
Publication Date: 2023-10-30
DOI: 10.1016/j.bbrc.2023.08.050

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2

Publication Name: The Journal of biological chemistry
Publication Date: 2022-08
DOI: 10.1016/j.jbc.2022.102228

A review on the synthesis of heteroannulated quinolones and their biological activities

Publication Name: Molecular Diversity
Publication Date: 2021-10-26
DOI: 10.1007/s11030-021-10332-1

Thiazole Synthesis by Thionation of C=O to C=S

Publication Name: Lawesson’s Reagent in Heterocycle Synthesis
Publication Date: 2021-09-11
DOI: 10.1007/978-981-16-4655-3_3