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2-(5-VINYL-1-AZABICYCLO[2,2,2]OCTAN-2-YL)INDOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61119-84-4

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61119-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61119-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,1 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61119-84:
(7*6)+(6*1)+(5*1)+(4*1)+(3*9)+(2*8)+(1*4)=104
104 % 10 = 4
So 61119-84-4 is a valid CAS Registry Number.

61119-84-4SDS

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-(5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl)-1H-indole

1.2 Other means of identification

Product number -
Other names 2-(5-VINYL-1-AZABICYCLO[2,2,2]OCTAN-2-YL)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:61119-84-4 SDS

61119-84-4Downstream Products

61119-84-4Relevant academic research and scientific papers

ORGANOMETALLIC REAGENTS IN SYNTHESIS A NEW PROTOCOL FOR CONSTRUCTION OF THE INDOLE NUCLEUS

Smith, III, Amos B.,Visnick, Melean,Haseltine, John N.,Sprengeler, Paul A.

, p. 2957 - 2970 (2007/10/02)

Organodilithium reagents derived from 2-alkyl-N-trimethylsilyl anilines undergo condensation with esters of carboxylic acids to afford substituted indoles.A total of 16 examples are reported; yields in general were good.In conjuction with this program, a convenient, large-scale procedure for preparation of monosilylated anilines was also developed.To demonstrate the utility of the new indole protocol in natural products synthesis, efficient syntheses of (+)-cinchonamine and (+)-epi-cinchonamine as well as a tetracyclic model system for the architecturally complex penitrem mycotoxins were completed in regio- and stereoselective fashion.

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