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65134-44-3

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65134-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65134-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,3 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65134-44:
(7*6)+(6*5)+(5*1)+(4*3)+(3*4)+(2*4)+(1*4)=113
113 % 10 = 3
So 65134-44-3 is a valid CAS Registry Number.

65134-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-phenoxy-3-phenylacrylonitrile

1.2 Other means of identification

Product number -
Other names β-Phenoxy-zimtsaeure-nitril

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:65134-44-3 SDS

65134-44-3Relevant articles and documents

Copper-catalyzed direct cyanation of terminal alkynes with benzoyl cyanide

Du, Yan,Li, Zheng

, p. 4622 - 4625 (2018/11/27)

Copper-catalyzed direct cyanation of terminal alkynes is achieved using less toxic, stable and easy to handle benzoyl cyanide as a cyanide source and air as an oxidant. This protocol provides a good alternative to the preparation of 3-arylpropiolonitriles

Synthesis of (Z)-3-aryloxy-acrylonitriles, (E)-3-aryloxy-acrylonitriles and 3-cyanobenzofurans through the sequential reactions of phenols with propiolonitriles

Zhou, Wei,Zhang, Yicheng,Li, Pinhua,Wang, Lei

experimental part, p. 7184 - 7196 (2012/10/08)

A Na2CO3-promoted addition of phenols to propiolonitriles generated (Z)-3-aryloxy-acrylonitriles in nearly quantitative yields with exclusively Z-isomers, and a DABCO-promoted addition reaction of phenols with propiolonitriles afforded mainly (E)-3-aryloxy-acrylonitriles with high yields. The obtained (E)-3-aryloxy-acrylonitriles underwent intramolecular cyclization to give 3-cyanobenzofurans in good yields through palladium-catalyzed direct C-H bond functionalization.

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