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Benzoic acid, 4-chloro-2-hydrazino(9CI) is an organic compound with the molecular formula C7H6ClN3O. It is derived from benzoic acid, featuring a chlorine atom at the 4-position and a hydrazino group at the 2-position. Benzoic acid, 4-chloro-2-hydrazino(9CI) has been studied for its potential applications in various fields due to its unique chemical structure and properties.

299166-41-9

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299166-41-9 Usage

Uses

Used in Pharmaceutical Industry:
Benzoic acid, 4-chloro-2-hydrazino(9CI) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Research and Development:
In the field of research and development, Benzoic acid, 4-chloro-2-hydrazino(9CI) is utilized as a starting material for the exploration of new chemical reactions and the synthesis of novel compounds. Its reactivity and structural features make it a valuable tool for advancing scientific knowledge and discovering new applications.
Used in the Study of BKCa Channel Openers:
Benzoic acid, 4-chloro-2-hydrazino(9CI) has been found in a study of benzofuroindole analogues as potent BKCa channel openers. BKCa channels are important targets for the treatment of various diseases, including hypertension, diabetes, and neurological disorders. As a compound with potential activity in this area, it may contribute to the development of new therapeutic agents for these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 299166-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,1,6 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 299166-41:
(8*2)+(7*9)+(6*9)+(5*1)+(4*6)+(3*6)+(2*4)+(1*1)=189
189 % 10 = 9
So 299166-41-9 is a valid CAS Registry Number.

299166-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2-hydrazinobenzoic acid

1.2 Other means of identification

Product number -
Other names -

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:299166-41-9 SDS

299166-41-9Upstream product

299166-41-9Downstream Products

299166-41-9Relevant academic research and scientific papers

Bacterial translation inhibitors, 1-acylindazol-3-ols as anthranilic acid mimics

Stiff, Cory,Graber, David R.,Thorarensen, Atli,Wakefield, Brian D.,Marotti, Keith R.,Melchior, Earline P.,Sweeney, Michael T.,Han, Fusen,Rohrer, Douglas C.,Zurenko, Gary E.,Romero, Donna L.

scheme or table, p. 6293 - 6297 (2009/07/18)

The discovery and initial optimization of a novel anthranilic acid derived class of antibacterial agents has been described in a recent series of papers. This paper describes the discovery of 1-acylindazol-3-ols as a novel bioisostere of an anthranilic acid. The synthesis and structure-activity relationships of the indazol bioisosteres are described herein.

4,5-Dihydro-5-oxopyrazolo[1,5-a]quinazoline-3-carboxylic acid derivatives

-

, (2008/06/13)

4,5-Dihydro-5-oxopyrazolo[1,5-a]quinazoline-3-carboxylic acids and esters and alkali metal salts thereof, useful as anti-inflammatory, anti-allergic and anti-parasitic agents, are prepared by reacting a 4- or 5-R3 -2-carboxyphenylhydrazine with a lower-alkyl ethoxymethylenecyanoacetate and, if desired, saponifying the ester group and if desired, N-alkylating the product by reaction with an R2 -halide in the presence of an acid-acceptor.

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