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(2Z)-3-(3-chlorophenyl)-2-(4-chlorophenyl)prop-2-enenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93986-80-2

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93986-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93986-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,8 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93986-80:
(7*9)+(6*3)+(5*9)+(4*8)+(3*6)+(2*8)+(1*0)=192
192 % 10 = 2
So 93986-80-2 is a valid CAS Registry Number.

93986-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-(3-chlorophenyl)-2-(4-chlorophenyl)acrylonitrile

1.2 Other means of identification

Product number -
Other names (Z)-3-(3-chloro-phenyl)-2-(4-chloro-phenyl)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:93986-80-2 SDS

93986-80-2Downstream Products

93986-80-2Relevant academic research and scientific papers

MDM2-HDAC double-target inhibitor, medicinal composition and preparation and application of MDM2-HDAC double-target inhibitor

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Paragraph 0207-0209, (2018/12/14)

The invention provides a MDM2-HDAC double-target inhibitor, a medicinal composition and preparation and application of the MDM2-HDAC double-target inhibitor. The MDM2-HDAC double-target inhibitor hasa structure as shown in formula I. The inhibitor with th

Discovery of RG7388, a potent and selective p53-MDM2 inhibitor in clinical development

Ding, Qingjie,Zhang, Zhuming,Liu, Jin-Jun,Jiang, Nan,Zhang, Jing,Ross, Tina M.,Chu, Xin-Jie,Bartkovitz, David,Podlaski, Frank,Janson, Cheryl,Tovar, Christian,Filipovic, Zoran M.,Higgins, Brian,Glenn, Kelli,Packman, Kathryn,Vassilev, Lyubomir T.,Graves, Bradford

supporting information, p. 5979 - 5983 (2013/08/23)

Restoration of p53 activity by inhibition of the p53-MDM2 interaction has been considered an attractive approach for cancer treatment. However, the hydrophobic protein-protein interaction surface represents a significant challenge for the development of s

N-SUBSTITUTED PYRROLIDINES

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Page/Page column 11, (2012/01/15)

Compounds of formula and enantiomers and pharmaceutically acceptable salts thereof are described, as well as the pharmaceutical compositions containing said compounds and their pharmaceutically acceptable salts, and the use of said compounds and pharmaceu

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