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118645-77-5

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118645-77-5 Usage

Molecular weight

142.56 g/mol This is the mass of one mole of the compound, which is a measure of its size and stability.
Commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds This describes the compound's use in the production of other chemicals, particularly in the pharmaceutical and organic chemistry industries.
Studied for its potential applications in the field of organic electronics This indicates that the compound has potential uses in the development of electronic devices made from organic materials.
Potential toxicity and reactivity This warns of the possible dangers associated with the compound, which require proper safety precautions and handling procedures to be followed.

Check Digit Verification of cas no

The CAS Registry Mumber 118645-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,4 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 118645-77:
(8*1)+(7*1)+(6*8)+(5*6)+(4*4)+(3*5)+(2*7)+(1*7)=145
145 % 10 = 5
So 118645-77-5 is a valid CAS Registry Number.

118645-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-amino-2-chloroethylidene)propanedinitrile

1.2 Other means of identification

Product number -
Other names 2-(1-amino-2-chloroethylidene)malononitrile

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:118645-77-5 SDS

118645-77-5Relevant articles and documents

NEW ONE-POT SYNTHESIS OF ENAMINEDINITRILES

Berry, Robert W. H.,Drewry, Peter C.,Hodson, Harold F.

, p. 958 - 975 (2007/10/02)

A convenient procedure is reported for the one-pot preparation of enaminedinitriles.This involves the sodium methoxide-catalysed addition of methanol to a suitably substituted nitrile followed by reaction of the resulting imidate with malononitrile.The mechanism, scope and limitations of the synthesis have been investigated.Spectroscopic evidence is presented that the products exist in the enaminedinitrile rather than in the tautomeric imino form.Various reactions of the compounds including halogen exchange, anion formation and amine displacement have been studied and used to extend the range of enaminedinitriles prepared.

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