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N-(3,5-dibromo-4-hydroxyphenyl)-2-hydroxybenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55411-39-7

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55411-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55411-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,1 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55411-39:
(7*5)+(6*5)+(5*4)+(4*1)+(3*1)+(2*3)+(1*9)=107
107 % 10 = 7
So 55411-39-7 is a valid CAS Registry Number.

55411-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,5-dibromo-4-hydroxyphenyl)-2-hydroxybenzamide

1.2 Other means of identification

Product number -
Other names 3',5'-Dibromo-2,4'-dihydroxybenzanilide

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:55411-39-7 SDS

55411-39-7Downstream Products

55411-39-7Relevant academic research and scientific papers

Improved compsn. antiallergic habitus

-

, (2007/10/06)

PROBLEM TO BE SOLVED: To provide a composition for ameliorating allergic constitution naturally ingestible in daily life. SOLUTION: The composition for ameliorating the allergic constitution comprises a galactooligosaccharide as a main ingredient. Furthermore, a food and drink uses the composition. Since the galactooligosaccharide is already widely used in heath-oriented foods such as a specific food for health and is a material in which the safety is sufficiently established, the galactooligosaccharide is naturally ingestible over a long period in the daily life. COPYRIGHT: (C)2007,JPOandINPIT

Toward optimization of the second aryl 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. 1115 - 1125 (2009/12/24)

Transthyretin (TTR) amyloidogenesis inhibitors are typically composed of two aromatic rings and a linker. We have previously established optimal structures for one aromatic ring and the linker. Herein, we employ a suboptimal linker and an optimal aryl-X substructure to rank order the desirability of aryl-Z substructures-using a library of 56 N-(3,5-dibromo-4-hydroxyphenyl) benzamides. Coconsideration of amyloid inhibition potency and ex vivo plasma TTR binding selectivity data reveal that 2,6, 2,5, 2, 3,4,5, and 3,5 substituted aryls bearing small substituents generate the most potent and selective inhibitors, in descending order. These benzamides generally lack undesirable thyroid hormone receptor binding and COX-1 inhibition activity. Three high-resolution TTR ? inhibitor crystal structures (1.31-1.35 ?) provide insight into why these inhibitors are potent and selective, enabling future structure-based design of TTR kinetic stabilizers.

Pharmaceutical method for the therapy of immune diseases

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, (2008/06/13)

Compounds having the formula STR1 (the meanings of R1, R2, R3, R4 and R5 are indicated hereinafter) exhibit suppressive activity to various immune responses and can be employed in the therapy of immun

Treatment of elevated histamine and uric acid levels

-

, (2008/06/13)

Compounds having the general formula SPC1 (the meanings of R1, R2, R3, R4 and R5 are indicated hereinafter) and the pharmaceutically acceptable salts and esters thereof exhibit strong activities in inhibiting histidine decarboxylase and xanthine oxidase. One example is the compound of the formula SPC2

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