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6-Hydroxy-5-azaindole is a chemical compound characterized by the molecular formula C7H6N2O. It is an aromatic heterocyclic organic compound, featuring a five-membered ring with a nitrogen atom. Known for its versatile reactivity and functional groups, 6-Hydroxy-5-azaindole serves as a fundamental building block in the synthesis of pharmaceuticals and agrochemicals. Its potential biological and medical applications, particularly as an anti-cancer agent, make 6-Hydroxy-5-azaindole a significant compound in the realm of organic chemistry and drug development, warranting further research and exploration for industrial applications.

70357-66-3

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70357-66-3 Usage

Uses

Used in Pharmaceutical Synthesis:
6-Hydroxy-5-azaindole is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the creation of a wide range of medicinal compounds, contributing to the development of new treatments and therapies.
Used in Agrochemical Production:
In the agrochemical industry, 6-Hydroxy-5-azaindole serves as a crucial component in the formulation of pesticides and other crop protection agents. Its incorporation enhances the effectiveness of these products, supporting agricultural productivity and crop health.
Used in Organic Chemistry Research:
6-Hydroxy-5-azaindole is employed as a model compound in organic chemistry research, facilitating the study of reaction mechanisms, synthetic pathways, and the exploration of novel chemical transformations.
Used in Drug Development:
6-Hydroxy-5-azaindole is used as a potential anti-cancer agent in drug development. Its biological activity and interaction with cellular targets are under investigation to assess its efficacy in combating cancer and its potential for integration into therapeutic strategies.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-Hydroxy-5-azaindole is applied as a structural motif for the design of new drug candidates. Its presence in molecular frameworks can influence pharmacokinetic and pharmacodynamic properties, guiding the optimization of lead compounds for specific therapeutic indications.

Check Digit Verification of cas no

The CAS Registry Mumber 70357-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,5 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70357-66:
(7*7)+(6*0)+(5*3)+(4*5)+(3*7)+(2*6)+(1*6)=123
123 % 10 = 3
So 70357-66-3 is a valid CAS Registry Number.

70357-66-3SDS

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 1,5-dihydropyrrolo[3,2-c]pyridin-6-one

1.2 Other means of identification

Product number -
Other names 6-HYDROXY-5-AZAINDOLE

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:70357-66-3 SDS

70357-66-3Upstream product

70357-66-3Relevant academic research and scientific papers

Synthesis method of 1H-pyrrole [3, 2-c] pyridin-6-ol

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Paragraph 0024; 0028; 0030-0031; 0036-0040, (2020/12/09)

The invention provides a synthesis method of 1H-pyrrole [3, 2-c] pyridin-6-ol, and relates to the technical field of chemical intermediate synthesis; 6-chloro-5-azaindole is used as a raw material, alkali adding and acid binding are performed, and 6-(benzyloxy)-1H-pyrrolo [3, 2-c] pyridine is generated through reaction with benzyl alcohol. Hydrogenating and debenzylating are carried out 6-(benzyloxy)-1H-pyrrolo [3, 2-c] pyridine to obtain 1H-pyrrole [3, 2-c] pyridin-6-ol; according to the preparation method, the problem that 6-chloro-5-azaindole is chlorinated into hydroxyl is effectively solved, and a 1H-pyrrole [3, 2-c] pyridin-6-ol product is successfully prepared; and the method provided by the invention has the advantages of short route, commercially available raw material reagent, nouse of dangerous and toxic chemical reagent, mild reaction conditions, simple operation and easy scale-up production.

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