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QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is a hydrazide derivative of quinoline carboxylic acid with the molecular formula C10H8N2O2. It is a chemical compound commonly used in organic synthesis and as a building block in the production of pharmaceuticals, agrochemicals, and dyes.

96541-83-2

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96541-83-2 Usage

Uses

Used in Pharmaceutical Industry:
QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is used as a building block for the development of pharmaceuticals due to its versatile chemical properties and potential therapeutic applications.
Used in Agrochemical Industry:
QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is used as a building block for the development of agrochemicals, contributing to its potential use in pest control and crop protection.
Used in Dye Industry:
QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is used as a building block in the synthesis of dyes, providing a range of colorants for various applications.
Used in Antitubercular Applications:
QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is used as a potential antitubercular agent, exhibiting properties that can be harnessed for the development of new treatments against tuberculosis.
Used in Antimicrobial Applications:
QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is used as a potential antimicrobial agent, showing promise in the development of new treatments against various microbial infections.
Used in Corrosion Inhibition:
QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is used as a potential corrosion inhibitor, with studies exploring its ability to protect materials from corrosion in various industrial applications.
Used in Organic Synthesis:
QUINOLINE-5-CARBOXYLIC ACID HYDRAZIDE is used as an intermediate in the synthesis of complex organic compounds, contributing to the development of new chemical entities with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 96541-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,4 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96541-83:
(7*9)+(6*6)+(5*5)+(4*4)+(3*1)+(2*8)+(1*3)=162
162 % 10 = 2
So 96541-83-2 is a valid CAS Registry Number.

96541-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name quinoline-5-carbohydrazide

1.2 Other means of identification

Product number -
Other names quinoline-5-carboxylic acid hydrazide

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:96541-83-2 SDS

96541-83-2Relevant academic research and scientific papers

INDOLE COMPOUNDS AS ANDROGEN RECEPTOR MODULATORS

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Page/Page column 40; 51, (2022/02/05)

Provided herein are compounds of formula (V) that bind to BF3 of an androgen receptor (AR), which can modulate the AR for the treatment of Kennedy's disease.

Discovery of potent and selective inhibitors of human reticulocyte 15-lipoxygenase-1

Rai, Ganesha,Kenyon, Victor,Jadhav, Ajit,Schultz, Lena,Armstrong, Michelle,Jameson, J. Brian,Hoobler, Eric,Leister, William,Simeonov, Anton,Holman, Theodore R.,Maloney, David J.

scheme or table, p. 7392 - 7404 (2011/01/12)

There are a variety of lipoxygenases in the human body (hLO), each having a distinct role in cellular biology. Human reticulocyte 15-lipoxygenase-1 (15-hLO-1), which catalyzes the dioxygenation of 1,4-cis,cis-pentadiene- containing polyunsaturated fatty acids, is implicated in a number of diseases including cancer, atherosclerosis, and neurodegenerative conditions. Despite the potential therapeutic relevance of this target, few inhibitors have been reported that are both potent and selective. To this end, we have employed a quantitative high-throughput (qHTS) screen against ~74000 small molecules in search of reticulocyte 15-hLO-1 selective inhibitors. This screen led to the discovery of a novel chemotype for 15-hLO-1 inhibition, which displays nM potency and is >7500-fold selective against the related isozymes, 5-hLO, platelet 12-hLO, epithelial 15-hLO-2, ovine cyclooxygenase-1, and human cyclooxygenase-2. In addition, kinetic experiments were performed which indicate that this class of inhibitor is tight binding, reversible, and appears not to reduce the active-site ferric ion.

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