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40846-65-9

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40846-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40846-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,4 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40846-65:
(7*4)+(6*0)+(5*8)+(4*4)+(3*6)+(2*6)+(1*5)=119
119 % 10 = 9
So 40846-65-9 is a valid CAS Registry Number.

40846-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-isocyanobutanoate

1.2 Other means of identification

Product number -
Other names methyl 2-isocyanobutyrate

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:40846-65-9 SDS

40846-65-9Relevant articles and documents

A resource-efficient and highly flexible procedure for a three-component synthesis of 2-imidazolines

Elders, Niels,Schmitz, Rob F.,De Kanter, Frans J. J.,Ruijter, Eelco,Groen, Marinus B.,Orru, Romano V. A.

, p. 6135 - 6142 (2008/02/10)

(Chemical Equation Presented) A multicomponent reaction between α-acidic isonitriles, primary amines, and carbonyl compounds was studied using 14 different solvents. Depending on the isocyanide that was used, optimal yields for the three-component synthesis of 2H-2-imidazolines were observed in different solvents. The solvents could be used as purchased, and in situ preformation of the imine was not required. By selecting the appropriate solvent, it was possible to considerably expand the range of compatible isocyanides toward less α-acidic isocyanides. Further process simplification was achieved by performing the reaction at higher concentrations and avoiding purification by column chromatography, resulting in a fast, easy to perform, and resource-efficient protocol for this three-component reaction.

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