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93863-65-1

2-Propenenitrile, 3-(1-naphthalenyl)-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93863-65-1

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93863-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93863-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,8,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93863-65:
(7*9)+(6*3)+(5*8)+(4*6)+(3*3)+(2*6)+(1*5)=171
171 % 10 = 1
So 93863-65-1 is a valid CAS Registry Number.

93863-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1-(acrylonitrile-3-yl)naphthalene

1.2 Other means of identification

Product number -
Other names (E)-3-Naphthalen-1-yl-acrylonitrile

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:93863-65-1 SDS

93863-65-1Downstream Products

93863-65-1Relevant articles and documents

Palladium-Catalyzed Arylation of Unsymmetrical Olefins. Bidentate Phosphine Ligand Controlled Regioselectivity

Cabri, Walter,Candiani, Ilaria,Bedeschi, Angelo,Santi, Roberto

, p. 3558 - 3563 (1992)

The palladium-catalyzed arylation of several unsymmetrical olefins by aryl triflates in the presence of bidentate phosphine ligands is described.The use of these ligands increases the influence that electronic factors have in determining the regioselectivity of the reaction.The catalyst performances allow a revisiting of the scheme that describes the regioselectivity outcome in Heck-type reactions.Furthermore, a general mechanism for the palladium-catalyzed arylation of olefins is proposed.

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