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16610-81-4

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16610-81-4 Usage

Uses

a-(p-Chlorophenyl)cinnamonitrile is used in the synthesis of lamellarins O and Q.

Check Digit Verification of cas no

The CAS Registry Mumber 16610-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,1 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16610-81:
(7*1)+(6*6)+(5*6)+(4*1)+(3*0)+(2*8)+(1*1)=94
94 % 10 = 4
So 16610-81-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClN/c16-15-8-6-13(7-9-15)14(11-17)10-12-4-2-1-3-5-12/h1-10H

16610-81-4 Well-known Company Product Price

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  • Alfa Aesar

  • (B25644)  (E)-alpha-(4-Chlorophenyl)cinnamonitrile, 99%   

  • 16610-81-4

  • 5g

  • 644.0CNY

  • Detail
  • Alfa Aesar

  • (B25644)  (E)-alpha-(4-Chlorophenyl)cinnamonitrile, 99%   

  • 16610-81-4

  • 25g

  • 2269.0CNY

  • Detail

16610-81-4SDS

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 (Z)-2-(4-chlorophenyl)-3-phenylprop-2-enenitrile

1.2 Other means of identification

Product number -
Other names 2-(4-Chlor-phenyl)-3-phenyl-acrylonitril

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:16610-81-4 SDS

16610-81-4Relevant articles and documents

Synthesis of non-symmetrical 3,4-diaryl-substituted pyrroles: Implementation for the preparation of lamellarin R

Zavala-Gómez, Héctor,Ramírez-Rodríguez, Armando,Vázquez, Alfredo

, p. 677 - 683 (2018/01/08)

A straightforward method for synthesising symmetrical and non-symmetrical 3,4-diaryl-substituted pyrroles is proposed, consisting of (i) the condensation reaction between phenylacetonitriles and aldehydes to give acrylonitriles, (ii) the conjugate additio

A process for preparing two aromatic ring substituted olefins method

-

Paragraph 0049-0051, (2017/06/08)

The invention relates to an efficient environment-friendly catalyst, and a new method for preparing double-(hetero)aromatic-ring substituted alkene under a room-temperature condition by taking water as a reaction medium. The method comprises: taking n-propylamine supported by super-paramagnetism nanometer particles and modified by ion atmosphere as a catalyst, and under the conditions of room temperature, normal pressure and water reaction medium, performing Knoevenagel condensation reaction on an (hetero)aromatic-ring substituted active alkene substance and an aromatic aldehyde, so as to obtain a corresponding double-(hetero)aromatic-ring substituted alkene derivative. The reaction yield is not obviously reduced after the supported catalyst is repeatedly used for 8 times. The method is simple in operation, high in yield, simple in catalyst recovery, good in reusability of the catalytic reaction system and mild in reaction conditions, and has good industrialization prospect.

Design of Bcl-2 and Bcl-xL inhibitors with subnanomolar binding affinities based upon a new scaffold

Zhou, Haibin,Chen, Jianfang,Meagher, Jennifer L.,Yang, Chao-Yie,Aguilar, Angelo,Liu, Liu,Bai, Longchuan,Cong, Xin,Cai, Qian,Fang, Xueliang,Stuckey, Jeanne A.,Wang, Shaomeng

experimental part, p. 4664 - 4682 (2012/07/28)

Employing a structure-based strategy, we have designed a new class of potent small-molecule inhibitors of the anti-apoptotic proteins Bcl-2 and Bcl-xL. An initial lead compound with a new scaffold was designed based upon the crystal structure of Bcl-xL an

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