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QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE is a chemical compound with the molecular formula C10H9N3O2, featuring a quinoline ring with a carboxylic acid group and a hydrazide functional group attached. It is a hydrazide derivative of quinoline-4-carboxylic acid, known for its potential antimicrobial, antitumor, and antiviral activities, as well as its applications in the synthesis of pharmaceuticals, agrochemicals, dyes, and pigments.

435271-32-2

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435271-32-2 Usage

Uses

Used in Pharmaceutical Industry:
QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE is used as a building block for the synthesis of various pharmaceuticals due to its potential antimicrobial and antitumor activities. Its derivative compounds have shown promise as inhibitors of protein kinase and enzyme activity, making it valuable in drug discovery and development.
Used in Agrochemical Industry:
In the agrochemical industry, QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE serves as a key component in the synthesis of agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used in Dye and Pigment Production:
QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE is utilized in the production of dyes and pigments, where its unique chemical structure imparts color and stability to various materials.
Used in Antimicrobial Applications:
QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE has been studied for its potential antimicrobial properties, making it a candidate for use in applications requiring the inhibition of microbial growth, such as in medical and industrial settings.
Used in Antitumor Research:
With its demonstrated antitumor activities, QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE is explored for its potential use in cancer treatment, targeting and inhibiting the growth of tumor cells.
Used in Antiviral Studies:
QUINOLINE-4-CARBOXYLIC ACID HYDRAZIDE's antiviral properties have been investigated in research studies, suggesting its potential use in the development of antiviral therapies to combat viral infections.

Check Digit Verification of cas no

The CAS Registry Mumber 435271-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,5,2,7 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 435271-32:
(8*4)+(7*3)+(6*5)+(5*2)+(4*7)+(3*1)+(2*3)+(1*2)=132
132 % 10 = 2
So 435271-32-2 is a valid CAS Registry Number.

435271-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name isoquinoline-4-carbothioamide

1.2 Other means of identification

Product number -
Other names ISOQUINOLINE-4-THIOCARBOXYAMIDE

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:435271-32-2 SDS

435271-32-2Upstream product

435271-32-2Downstream Products

435271-32-2Relevant academic research and scientific papers

SUBSTITUTED THIAZOLE DERIVATIVES BEARING 3-PYRIDYL GROUPS, PROCESS FOR PREPARING THE SAME AND USE THEREOF

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Page/Page column 40, (2008/06/13)

The present invention provides a pharmaceutical composition having a steroid C17,20-lyase inhibitory activity, which is useful as a prophylactic or therapeutic agent of prostatism, tumor such as breast cancer and the like, more particularly, a steroid C17,20-lyase inhibitor containing a compound represented by the formula: wherein A1 is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, one of A2 and A3 is a hydrogen atom, a halogen atom, a C1-4 aliphatic hydrocarbon group optionally having substituents or an optionally esterified carboxyl group, the other of A2 and A3 is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, and at least one of A1, A2 and A3 is a 3-pyridyl group optionally having substituents, or a salt thereof or a prodrug thereof.

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