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3,4-dibromo-1-(2-phenylethyl)-1H-pyrrole-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92751-35-4

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92751-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92751-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,5 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92751-35:
(7*9)+(6*2)+(5*7)+(4*5)+(3*1)+(2*3)+(1*5)=144
144 % 10 = 4
So 92751-35-4 is a valid CAS Registry Number.

92751-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dibromo-1-(2-phenylethyl)pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 3,4-dibromo-1-phenethylpyrrole-2,5-dione

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:92751-35-4 SDS

92751-35-4Relevant academic research and scientific papers

Development of antiproliferative phenylmaleimides that activate the unfolded protein response

Muus, Ulrike,Hose, Curtis,Yao, Wei,Kosakowska-Cholody, Teresa,Farnsworth, David,Dyba, Marzena,Lountos, George T.,Waugh, David S.,Monks, Anne,Burke Jr., Terrence R.,Michejda, Christopher J.

supporting information; experimental part, p. 4535 - 4541 (2010/08/22)

The current paper presents the synthesis and evaluation of a series of maleimides that were designed to inhibit the Cdc25 phosphatase by alkylation of catalytically essential cysteine residues. Although in HepB3 cell culture assays the analogues did exhib

Synthesis of substituted bis(heteroaryl)maleimides

Dubernet, Mathieu,Caubert, Virginie,Guillard, Jér?me,Viaud-Massuard, Marie-Claude

, p. 4585 - 4593 (2007/10/03)

Substituted bis(fur-2-yl), bis(fur-3-yl) and bis(thien-2-yl) maleimides with potential antidiabetic properties are described. Their synthesis involves, as a key step, a Suzuki cross-coupling between various boron derivatives and the diiodomaleimides. Therefore, a wide range of substituted symmetric and non-symmetric maleimide derivatives can be prepared.

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