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Propanedinitrile, (3-bromophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

297745-45-0

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297745-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 297745-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,7,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 297745-45:
(8*2)+(7*9)+(6*7)+(5*7)+(4*4)+(3*5)+(2*4)+(1*5)=200
200 % 10 = 0
So 297745-45-0 is a valid CAS Registry Number.

297745-45-0SDS

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 2-(3-bromophenyl)propanedinitrile

1.2 Other means of identification

Product number -
Other names 3-Bromophenylmalononitrile

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:297745-45-0 SDS

297745-45-0Relevant academic research and scientific papers

7,7-Dicyano-8,8-bis[4-(N,N-dimethylamino)phenyl]-meta-xylylenes: The first stable zwitterionic metaxylylene derivatives

Kawase, Takeshi,Iwata, Tohru,Oda, Masaji

, p. 322 - 323 (2003)

Treatment of 3-lithiophenyldicyanomethide ions with Michler's ketone afforded the title compounds as stable crystals upon weak-acidic work-up. The molecular structure and spectroscopic data reveal the zwitterionic nature of the compounds.

Beyond U0126. Dianion chemistry leading to the rapid synthesis of a series of potent MEK inhibitors

Wityak, John,Hobbs, Frank W.,Gardner, Daniel S.,Santella III, Joseph B.,Petraitis, Joseph J.,Sun, Jung-Hui,Favata, Margaret F.,Daulerio, Andrea J.,Horiuchi, Kurumi Y.,Copeland, Robert A.,Scherle, Peggy A.,Jaffe, Bruce D.,Trzaskos, James M.,Magolda, Ronald L.,Trainor, George L.,Duncia, John V.

, p. 1483 - 1486 (2007/10/03)

Employing phenylmalonitrile dianion chemistry, a large number of analogues of MEK inhibitor lead SH053 (IC50=140 nM) were rapidly synthesized leading to single digit nM inhibitors, displaying submicromolar AP-1 transcription inhibition in COS-7 cells. Compound 41, exhibiting a MEK IC 50=12 nM showed ip activity in a TPA-induced ear edema model with an ED50=5 mg/kg.

Amino-thio-acrylonitriles as MEK inhibitors

-

Page column 21, (2010/02/05)

This invention relates generally to amino-thio-acrylonitriles of formula Ia or Ib: as MEK inhibitors, pharmaceutical compositions containing the same, and methods of using the same as for treatment and prevention of inflammatory disorders or as an antican

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