71572-36-6 Usage
Description
1-benzyl-3,5-dibromobenzene is a chemical compound with the molecular formula C14H11Br2. It is a substituted benzene with two bromine atoms and a benzyl group attached to the benzene ring. 1-benzyl-3,5-dibromobenzene is known for its unique chemical properties and is commonly used in various applications across different industries.
Uses
Used in Organic Synthesis:
1-benzyl-3,5-dibromobenzene is used as a building block for the preparation of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a versatile intermediate in the synthesis of a wide range of organic compounds.
Used in Specialty Chemicals Production:
1-benzyl-3,5-dibromobenzene is used as an intermediate in the production of dyes, pigments, and other specialty chemicals. Its presence in these applications is due to its ability to impart specific properties to the final products, such as color, stability, and reactivity.
Used in Pharmaceutical Industry:
1-benzyl-3,5-dibromobenzene is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
1-benzyl-3,5-dibromobenzene is used as a building block for the preparation of agrochemicals, such as pesticides and herbicides. Its role in these applications is to provide the necessary chemical properties that enable the effective control of pests and weeds in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 71572-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,7 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71572-36:
(7*7)+(6*1)+(5*5)+(4*7)+(3*2)+(2*3)+(1*6)=126
126 % 10 = 6
So 71572-36-6 is a valid CAS Registry Number.
71572-36-6Relevant articles and documents
Aza-and polyaza-naphthalenly ketones useful as hiv integrase inhibitors
-
Page/Page column 51, (2010/02/10)
Certain aza- and polyaza-naphthalenyl ketones including certain quinolinyl and naphthyridinyl ketones 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 or the delay in the onset of AIDS, as compounds or pharmaceutically acceptable salts, or as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.
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
