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Propanedinitrile, (1-phenylpentyl)-2-propenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112654-16-7

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112654-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112654-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,5 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112654-16:
(8*1)+(7*1)+(6*2)+(5*6)+(4*5)+(3*4)+(2*1)+(1*6)=97
97 % 10 = 7
So 112654-16-7 is a valid CAS Registry Number.

112654-16-7SDS

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-(1-phenylpentyl)-2-prop-1-enylpropanedinitrile

1.2 Other means of identification

Product number -
Other names Propanedinitrile,(1-phenylpentyl)-2-propenyl

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:112654-16-7 SDS

112654-16-7Downstream Products

112654-16-7Relevant academic research and scientific papers

β-alkyl-α-allylation of Michael acceptors through the palladium-catalyzed three-component coupling between allylic substrates, trialkylboranes, and activated olefins

Patil, Nitin T.,Huo, Zhibao,Yamamoto, Yoshinori

, p. 2503 - 2506 (2006)

The palladium-catalyzed three-component β-alkyl-α-allylation reaction of activated olefins has been achieved. For example, in the presence of 5 mol % of Pd(PPh3)4, the reaction of benzylidenemalononitrile 1a with Et3B and allyl acetate 2a in THF proceeded smoothly at 40 °C to give the corresponding β-ethyl-α- allylated product 3a in 81% yield.

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