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90322-71-7

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90322-71-7 Usage

General Description

2-Carboxy-6-nitrobenzeneacetic acid, also known as "Carboxynitrobenzene", is a chemical compound used in the synthesis of pharmaceuticals and agrochemicals. It is a yellow crystalline substance with a molecular formula of C9H7NO6 and a molecular weight of 225.16 g/mol. 2-Carboxy-6-nitrobenzeneacetic acid is known for its anti-inflammatory and analgesic properties and is used in the manufacturing of non-steroidal anti-inflammatory drugs (NSAIDs) such as diclofenac. 2-Carboxy-6-nitrobenzeneacetic acid is also used as an intermediate in the production of dyes, pigments, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 90322-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90322-71:
(7*9)+(6*0)+(5*3)+(4*2)+(3*2)+(2*7)+(1*1)=107
107 % 10 = 7
So 90322-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO6/c1-2-17-10(14)8-6(9(12)13)4-3-5-7(8)11(15)16/h3-5H,2H2,1H3,(H,12,13)

90322-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(carboxymethyl)-3-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Nitro-homophthalsaeure

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:90322-71-7 SDS

90322-71-7Relevant articles and documents

Identification of novel PARP-1 inhibitors: Drug design, synthesis and biological evaluation

Xie, Zhouling,Zhou, Youli,Zhao, Wei,Jiao, He,Chen, Yu,Yang, Yong,Li, Zhiyu

supporting information, p. 4557 - 4561 (2015/10/12)

A series of AG014699 derivatives containing a novel scaffold of 2,3-dihydro-1H-[1,2]diazepino[4,5,6-cd]indole-1,4(6H)-dione were synthesized and evaluated for their inhibitory activities toward PARP-1 enzyme and two cell lines, MCF-7 cells and the BRCA1-deficient MDA-MB-436 cells. Our results demonstrated that of all AG014699 derivatives synthesized in this work, compounds 6 and 7 showed strong PARP-1 inhibitory activity (IC50 = 3.5 nM and 2.4 nM, respectively), only four and three times less potent than AG014699. Compound 6 also had significantly cell inhibitory activity against both MCF-7 cells (CC50 = 25.8 μM) and the BRCA1-deficient MDA-MB-436 cells (CC50 = 5.4 μM), nearly as good as AG014699, indicating that it can be a promising compound for further evaluation.

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