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183622-35-7

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183622-35-7 Usage

General Description

2-Nitro-5-piperazin-1-yl-benzoic acid is a chemical compound with the molecular formula C13H14N4O4. It is a nitrobenzoic acid derivative with a piperazine ring attached to its structure. 2-NITRO-5-PIPERAZIN-1-YL-BENZOIC ACID is used for its pharmaceutical properties, primarily as an intermediate in the synthesis of potential drug candidates. It has shown to possess anti-cancer and anti-inflammatory properties and is being researched for its potential use in the treatment of various diseases. Additionally, it has been found to have antimicrobial and antifungal activities, making it a versatile compound with potential applications in medicine and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 183622-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,6,2 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 183622-35:
(8*1)+(7*8)+(6*3)+(5*6)+(4*2)+(3*2)+(2*3)+(1*5)=137
137 % 10 = 7
So 183622-35-7 is a valid CAS Registry Number.

183622-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-5-piperazin-1-ylbenzoic acid

1.2 Other means of identification

Product number -
Other names F2147-0703

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:183622-35-7 SDS

183622-35-7Relevant articles and documents

BICYCLIC QUINAZOLINONE DERIVATIVES

-

Page/Page column 53-54, (2016/10/31)

The invention provides novel compounds having the general formula (I) wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R12, R13, R14, A1, A2, A3, n and m are as described herein.

Non-peptide glycoprotein IIb/IIIa antagonists. 11. Design and in vivo evaluation of 3,4-dihydro-1(1H)-isoquinolinone-based antagonists and ethyl ester prodrugs

Hutchinson, John H.,Cook, Jacquelynn J.,Brashear, Karen M.,Breslin, Michael J.,Glass, Joan D.,Gould, Robert J.,Halczenko, Wasyl,Holahan, Marie A.,Lynch, Robert J.,Sitko, Gary R.,Stranieri, Maria T.,Hartman, George D.

, p. 4583 - 4591 (2007/10/03)

The structure-activity relationship of a series of orally active glycoprotein IIb/IIIa antagonists containing a nitrogen heterocycle grafted onto a 3,4-dihydro-1(1H)-isoquinolinone core is described. These compounds are structurally novel analogs of the p

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