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Ethanone, 2-chloro-1-(1H-indol-6-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123216-45-5

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123216-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123216-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,1 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 123216-45:
(8*1)+(7*2)+(6*3)+(5*2)+(4*1)+(3*6)+(2*4)+(1*5)=85
85 % 10 = 5
So 123216-45-5 is a valid CAS Registry Number.

123216-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(1H-indol-6-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2-CHLORO-1-(1H-INDOL-6-YL)-ETHANONE

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:123216-45-5 SDS

123216-45-5Downstream Products

123216-45-5Relevant academic research and scientific papers

Regioselective acylations at the 2 and 6 position of N-acetylindole

Cruz, Rosimeire P.A.,Ottoni, Olívia,Abella, Carlos A.M.,Aquino, Lígia B.

, p. 1467 - 1469 (2001)

Regioselective acylations under Friedel-Crafts conditions at C6 and C2 positions of N-acetylindole are described.

INDOLE DERIVATIVES. 131.* REACTION OF 1-ACYLINDOLES WITH ACETYLCHLORIDE AND CHLOROACETYLCHLORIDE UNDER FRIEDEL-CRAFTS CONDITIONS

Shner, V.F.,Sladkova, T.N.,Turchin, K.F.,Suvorov, N.N.

, p. 272 - 274 (2007/10/02)

Acylation of 1-acylindoles by acetylchloride and chloroacetylchloride in the presence of aluminium chloride leads to formation of 3-acetyl and 6-chloroacetyl-1-acylindoles, respectively.

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