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2-(Chloromethyl)indolizine-1-carbonitrile is a chemical compound with the molecular formula C10H9ClN2. It is a derivative of indolizine and contains a chloromethyl and a carbonitrile group. 2-(CHLOROMETHYL)INDOLIZINE-1-CARBONITRILE is known for its potential applications in organic synthesis and drug discovery due to its reactivity and structural features. Its unique molecular structure and functional groups make it a valuable building block for the preparation of various organic compounds, including pharmaceuticals and agrochemicals. Additionally, its diverse reactivity allows for the synthesis of novel chemical entities with potential biological activities.

731821-82-2

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731821-82-2 Usage

Uses

Used in Organic Synthesis:
2-(Chloromethyl)indolizine-1-carbonitrile is used as a building block for the synthesis of various organic compounds. Its chloromethyl and carbonitrile groups provide opportunities for further chemical reactions, making it a versatile starting material for the creation of new molecules with potential applications in different fields.
Used in Drug Discovery:
2-(Chloromethyl)indolizine-1-carbonitrile is used as a key intermediate in the development of new pharmaceuticals. Its unique structure and reactivity enable the synthesis of novel chemical entities that may exhibit biological activities, such as therapeutic effects or interactions with biological targets. 2-(CHLOROMETHYL)INDOLIZINE-1-CARBONITRILE has the potential to contribute to the discovery of new drugs with useful properties for the treatment of various diseases.
Used in Agrochemical Development:
2-(Chloromethyl)indolizine-1-carbonitrile is used as a precursor in the synthesis of agrochemicals. Its structural features and reactivity make it a valuable component in the development of new pesticides, herbicides, or other agricultural chemicals that can improve crop protection and yield.
Used in Research and Development:
2-(Chloromethyl)indolizine-1-carbonitrile is used as a research compound in the exploration of new chemical reactions and the synthesis of novel molecules. Its potential for creating new chemical entities with diverse properties makes it an important tool in the advancement of scientific knowledge and the development of innovative materials and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 731821-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,1,8,2 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 731821-82:
(8*7)+(7*3)+(6*1)+(5*8)+(4*2)+(3*1)+(2*8)+(1*2)=152
152 % 10 = 2
So 731821-82-2 is a valid CAS Registry Number.

731821-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(CHLOROMETHYL)INDOLIZINE-1-CARBONITRILE

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:731821-82-2 SDS

731821-82-2Relevant articles and documents

[6,6] FUSED BICYCLIC HDAC8 INHIBITORS

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Paragraph 00370, (2019/08/15)

The present invention is directed to compounds of Formula I: and pharmaceutically acceptable salts, prodrugs, solvates, hydrates, tautomers, or isomers or thereof, wherein R1, R2, R2', L, X, W, Y1,Y2,

A new synthetic approach to pyrrolo[3,4-a]indolizines

Tereshchenko, Alexander D.,Sysoiev, Dmitry A.,Tverdokhlebov, Anton V.,Tolmachev, Andrey A.

, p. 349 - 353 (2007/10/03)

2-Pyridineacetonitrile was found to react with 1,3-dichloro-2-propanone in the presence of chlorotrimethylsilane yielding 2-chloromethyl-1- indolizinecarbonitrile. The chlorine atom in the prepared indolizine was replaced by various nucleophiles including

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