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40856-15-3

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40856-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40856-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,5 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40856-15:
(7*4)+(6*0)+(5*8)+(4*5)+(3*6)+(2*1)+(1*5)=113
113 % 10 = 3
So 40856-15-3 is a valid CAS Registry Number.

40856-15-3SDS

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 (Z)-non-2-enenitrile

1.2 Other means of identification

Product number -
Other names non-2c-enenitrile

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:40856-15-3 SDS

40856-15-3Downstream Products

40856-15-3Relevant articles and documents

Copper-catalyzed cyanation of alkenyl iodides

Nitelet, Antoine,Zahim, Sara,Theunissen, Cédric,Pradal, Alexandre,Evano, Gwilherm

, p. 163 - 177 (2017/03/06)

-

Highly active ruthenium-based catalyst for metathesis of cyano-contained olefins

Zhang, Wenzhen,Zhang, Rong,He, Ren

, p. 4203 - 4205 (2008/02/05)

Ruthenium benzylidene complex (H2IMes)(2-CH3-C5H4N)(Cl)2Ru{double bond, long}CHPh [H2IMes = 1,3-bis(2,6-dimethylphenyl)-4,5-dihydroimidazol-2-ylidene] (4), which introduced ortho substituted pyridine as dissociating ligand to weaken Ru-N bond and accelerate initiation through steric hindrance, was prepared by the reaction of (H2IMes)(PPh3)(Cl)2Ru{double bond, long}CHPh (1) with 2-methylpyridine and proved to exhibit enhanced catalytic activity for cyano-contained olefin metathesis.

Indium(I) bromide-mediated coupling of dibromoacetonitrile with aldehydes followed by Boord elimination of bromine and oxygen of β-bromo alkoxides for preparation of 3-organyl-2-alkenenitriles

Peppe, Clovis,de Azevedo Mello, Paola,das Chagas, Rafael Pav?o

, p. 2335 - 2339 (2007/10/03)

The organoindium compound derived from indium monobromide and dibromoacetonitrile reacts with carbonyl compounds to afford the corresponding 2-bromo-2-cyano-indium(III) alkoxide. The action of a second equivalent of indium monobromide onto the alkoxides derived from aldehydes promotes the Boord elimination of the β-related oxygen and bromine atoms leading to 2-alkenenitriles.

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