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3-(2-bromoanilino)-cyclohex-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68890-19-7

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68890-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68890-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,9 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68890-19:
(7*6)+(6*8)+(5*8)+(4*9)+(3*0)+(2*1)+(1*9)=177
177 % 10 = 7
So 68890-19-7 is a valid CAS Registry Number.

68890-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-bromoanilino)-cyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-(2-bromoanilino)-cyclohex-2-enone

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:68890-19-7 SDS

68890-19-7Relevant academic research and scientific papers

Process for the preparation of indoles

-

Page/Page column 4, (2008/06/13)

A process for the preparation of indoles, e.g. 1,2,3,9-tetrahydro-carbazol-4-one and derivatives thereof.

Condensed Heteroaromatic Ring Systems; XVII: Palladium-Catalyzed Cyclization of β-(2-Halophenyl)amino Substituted α,β-Unsaturated Ketones and Esters to 2,3-Disubstituted Indoles

Sakamoto, Takao,Nagano, Tatsuo,Kondo, Yoshinori,Yamanaka, Hiroshi

, p. 215 - 218 (2007/10/02)

Palladium-catalyzed cyclization of β-(2-halophenyl)amino substituted α,β-unsaturated ketones and esters, prepared from 2-haloanilines by three different methods, gave 2,3-disubstituted indoles.

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