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1214-09-1

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1214-09-1 Usage

Molecular weight

264.24 g/mol

Chemical structure

A compound containing an indole ring with a double bond and three cyano groups attached to it.

Appearance

Pale yellow or white solid.

Solubility

Insoluble in water, slightly soluble in methanol, and soluble in organic solvents like DMSO and acetonitrile.

Reactivity

Highly reactive due to the presence of the cyano groups and the double bond.

Uses

Primarily used in organic synthesis and chemical research as a building block for the preparation of various pharmaceuticals, agrochemicals, and other organic compounds.

Importance

Valuable due to its unique properties and potential applications in drug development, making it of particular interest to the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1214-09-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1214-09:
(6*1)+(5*2)+(4*1)+(3*4)+(2*0)+(1*9)=41
41 % 10 = 1
So 1214-09-1 is a valid CAS Registry Number.

1214-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1H-indol-3-yl)ethene-1,1,2-tricarbonitrile

1.2 Other means of identification

Product number -
Other names 2-(1H-indol-3-yl)-ethene-1,1,2-tricarbonitrile

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:1214-09-1 SDS

1214-09-1Downstream Products

1214-09-1Relevant articles and documents

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Shirota et al.

, p. 836,837, 838, 839 (1972)

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