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1H-Indole, 1-acetyl-7-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88150-28-1

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88150-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88150-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,5 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88150-28:
(7*8)+(6*8)+(5*1)+(4*5)+(3*0)+(2*2)+(1*8)=141
141 % 10 = 1
So 88150-28-1 is a valid CAS Registry Number.

88150-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(7-chloroindol-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1H-Indole,1-acetyl-7-chloro

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:88150-28-1 SDS

88150-28-1Downstream Products

88150-28-1Relevant academic research and scientific papers

Process for producing indoles unsubstituted in the 2,3-position and N(3-chloropropionyl)indole produced thereby

-

, (2008/06/13)

Indoles of the formula I which are unsubstituted in the 2- and 3-positions: STR1 wherein Z is hydrogen or a group --COR, and X and Y have the meanings defined in claim 1, can be produced by a novel, simple and economical process which comprises reacting a

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

Martin, Pierre

, p. 1647 - 1649 (2007/10/02)

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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