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3,5-dibromo-4-hydroxy-N-phenylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91805-70-8

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91805-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91805-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,0 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91805-70:
(7*9)+(6*1)+(5*8)+(4*0)+(3*5)+(2*7)+(1*0)=138
138 % 10 = 8
So 91805-70-8 is a valid CAS Registry Number.

91805-70-8SDS

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 3,5-dibromo-4-hydroxy-N-phenylbenzamide

1.2 Other means of identification

Product number -
Other names 3,5-dibromo-4-hydroxy-N-phenyl-benzamide

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:91805-70-8 SDS

91805-70-8Downstream Products

91805-70-8Relevant articles and documents

Toward optimization of the linker substructure common to transthyretin amyloidogenesis inhibitors using biochemical and structural studies

Johnson, Steven M.,Connelly, Stephen,Wilson, Ian A.,Kelly, Jeffery W.

supporting information; experimental part, p. 6348 - 6358 (2009/12/03)

To develop potent and highly selective transthyretin (TTR) amyloidogenesis inhibitors, it is useful to systematically optimize the three substructural elements that compose a typical TTR kinetic stabilizer: the two aryl rings and the linker joining them. Herein, we evaluated 40 bisaryl molecules based on 10 unique linker substructures to determine how these linkages influence inhibitor potency and selectivity. These linkers connect one unsubstituted aromatic ring to either a 3,5-X2 or a 3,5-X2-4-OH phenyl substructure (X = Br or CH3). Coconsideration of amyloid inhibition and ex vivo plasma TTR binding selectivity data reveal that direct connection of the two aryls or linkage through nonpolar E-olefin or -CH2CH2- substructures generates the most potent and selective TTR amyloidogenesis inhibitors exhibiting minimal undesirable binding to the thyroid hormone nuclear receptor or the COX-1 enzyme. Five high-resolution TTR·inhibitor crystal structures (1.4-1.8 A?) provide insight into why such linkers afford inhibitors with greater potency and selectivity.

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