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1H-Indole, 1-(chloroacetyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61995-53-7

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61995-53-7 Usage

Compound type

Derivative of indole, a heterocyclic aromatic compound

Substitution

Chloro-substituted indole with chloroacetyl group attached at the 1-position of the indole ring

Potential applications

Organic synthesis, medicinal chemistry, and drug discovery

Reactivity

High reactivity due to the presence of the chloroacetyl group

Biological activities

Diverse biological activities associated with indole derivatives

Handling precautions

Handle with caution, as it may possess certain hazards and can cause harm if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 61995-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,9 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61995-53:
(7*6)+(6*1)+(5*9)+(4*9)+(3*5)+(2*5)+(1*3)=157
157 % 10 = 7
So 61995-53-7 is a valid CAS Registry Number.

61995-53-7SDS

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 2-chloro-1-indol-1-ylethanone

1.2 Other means of identification

Product number -
Other names N1-(1-chloroacetyl)indole

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:61995-53-7 SDS

61995-53-7Downstream Products

61995-53-7Relevant academic research and scientific papers

192. Synthese von 2,3-unsubstituierten, N-acylierten Indolen durch sigmatrope-Umlagerung von O-Vinyl-N-phenylhydroxylaminderivaten

Martin, Pierre

, p. 1647 - 1649 (1984)

Treatment of N-phenylhydroxamic acids with vinylacetate in the presence of Li2PdCl4 affords 2,3-unsubstituted N-acylindoles via hetero-Cope-rearrangement of the intermediate N-phenyl-O-vinylhydroxylamine derivatives.

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