Cas 37795-93-0,4-bromo-N-(4-hydroxyphenyl)benzamide

37795-93-0

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Basic information

Product Name: 4-bromo-N-(4-hydroxyphenyl)benzamide
Synonyms: 4-bromo-N-(4-hydroxyphenyl)benzamide
CAS NO:37795-93-0
Molecular Formula: C₁₃H₁₀BrNO₂
Molecular Weight: 292.128
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-bromo-N-(4-hydroxyphenyl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-bromo-N-(4-hydroxyphenyl)benzamide(37795-93-0)
EPA Substance Registry System: 4-bromo-N-(4-hydroxyphenyl)benzamide(37795-93-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 37795-93-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 37795-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,9 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37795-93:
(7*3)+(6*7)+(5*7)+(4*9)+(3*5)+(2*9)+(1*3)=170
170 % 10 = 0
So 37795-93-0 is a valid CAS Registry Number.

37795-93-0Upstream product

37795-93-0Downstream Products

882738-23-0 4-bromo-N-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)benzamide

37795-93-0Relevant academic research and scientific papers

CATALYSTS FOR CHEMICAL REACTIONS IN A WATER-SURFACTANT MIXTURE

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Page/Page column 17-19, (2018/03/26)

The present invention is directed to reaction mixtures comprising a water-surfactant mixture, wherein the catalyst comprises a compound with solubilizing groups. This technology improves the solubility of the reaction components in the water-surfactant mi

Selective amidation of unprotected amino alcohols using surfactant-in-water technology: A highly desirable alternative to reprotoxic polar aprotic solvents

Parmentier, Michael,Wagner, Mona K.,Magra, Kevin,Gallou, Fabrice

supporting information, p. 1104 - 1107 (2017/01/16)

A general selective and environmentally friendly method for the formation of amide bonds using a surfactant in water as medium is described. The use of readily available 1-ethyl-3-(3-(dimethylamino)propyl)-carbodiimide (EDC) and hydroxybenzotriazol (HOBt)

Synthesis and SAR of piperazinyl-N-phenylbenzamides as inhibitors of hepatitis C virus RNA replication in cell culture

Conte, Immacolata,Giuliano, Claudio,Ercolani, Caterina,Narjes, Frank,Koch, Uwe,Rowley, Michael,Altamura, Sergio,Francesco, Raffaele De,Neddermann, Petra,Migliaccio, Giovanni,Stansfield, Ian

scheme or table, p. 1779 - 1783 (2009/12/03)

The RNA replication machinery of HCV is a multi-subunit membrane-associated complex. NS5A has emerged as an active component of HCV replicase, possibly involved in regulation of viral replication and resistance to the antiviral effect of interferon. We report here substituted piperazinyl-N-(aryl)benzamides as potent inhibitors of HCV replication exerted via modulation of the dimerization of NS5A.

MODULATORS OF HCV REPLICATION

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Page/Page column 17; 28, (2008/06/13)

The present invention is directed to the use of compounds of formula (I): 1 R X 3 R Y ( I) 2 R 5 where X, Y, R1, R2 and R3 are defined therein, which can act as modulators of viral replication and/or virus production, especially of the hepatitis C virus (HCV), in a cell based system.

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