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Benzenemethanol, 3-bromo-5-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

317334-60-4

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317334-60-4 Usage

Physical Form

White to off-white crystalline powder

Application

Used in the synthesis of pharmaceuticals and fine chemicals

Properties

Antimicrobial and Antiviral: Exhibits antimicrobial and antiviral properties
Starting Material: Commonly utilized as a starting material in the production of active pharmaceutical ingredients
Building Block: Acts as a building block in the synthesis of organic compounds
Reagent: Employed as a reagent in organic chemical reactions

Safety

Requires careful handling and storage due to potential health and environmental hazards

Check Digit Verification of cas no

The CAS Registry Mumber 317334-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,3 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 317334-60:
(8*3)+(7*1)+(6*7)+(5*3)+(4*3)+(3*4)+(2*6)+(1*0)=124
124 % 10 = 4
So 317334-60-4 is a valid CAS Registry Number.

317334-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-benzyl-5-bromo-phenyl)-methanol

1.2 Other means of identification

Product number -
Other names (3-Benzyl-5-bromo-phenyl)-methanol

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:317334-60-4 SDS

317334-60-4Relevant academic research and scientific papers

Design and synthesis of 8-hydroxy-[1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells

Zhuang, Linghang,Wai, John S.,Embrey, Mark W.,Fisher, Thorsten E.,Egbertson, Melissa S.,Payne, Linda S.,Guare Jr., James P.,Vacca, Joseph P.,Hazuda, Daria J.,Felock, Peter J.,Wolfe, Abigail L.,Stillmock, Kara A.,Witmer, Marc V.,Moyer, Gregory,Schleif, William A.,Gabryelski, Lori J.,Leonard, Yvonne M.,Lynch Jr., Joseph J.,Michelson, Stuart R.,Young, Steven D.

, p. 453 - 456 (2007/10/03)

Naphthyridine 7 inhibits the strand transfer of the integration process catalyzed by integrase with an IC50 of 10 nM and inhibits 95% of the spread of HIV-1 infection in cell culture at 0.39 μM. It does not exhibit cytotoxicity in cell culture

1-(Aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof

-

, (2010/02/06)

Certain 1-(aromatic- or heteroaromatic-substituted-3-(heteroaromatic substituted)-1,3-propanediones are described as inhibitors of HIV integrase and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HIV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.

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