736992-49-7 Usage
Uses
Used in Medicinal Chemistry:
1-[2-(Benzyloxy)-5-bromophenyl]adamantane is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its adamantane core and functional groups enable it to form specific interactions with biological targets, which can be exploited in the development of new drugs.
Used in Drug Discovery:
1-[2-(Benzyloxy)-5-bromophenyl]adamantane is used as a potential lead compound in drug discovery. Its unique structure and functional groups can be optimized to enhance its interactions with biological targets, leading to the development of new therapeutic agents.
Used in Chemical Research:
1-[2-(Benzyloxy)-5-bromophenyl]adamantane is used as a research tool in chemical research to study the interactions between chemical compounds and biological targets. Understanding these interactions can provide insights into the design and development of new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 736992-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,9,9 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 736992-49:
(8*7)+(7*3)+(6*6)+(5*9)+(4*9)+(3*2)+(2*4)+(1*9)=217
217 % 10 = 7
So 736992-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C23H25BrO/c24-20-6-7-22(25-15-16-4-2-1-3-5-16)21(11-20)23-12-17-8-18(13-23)10-19(9-17)14-23/h1-7,11,17-19H,8-10,12-15H2/t17-,18-,19-,23-
736992-49-7Relevant academic research and scientific papers
An adamantyl-substituted retinoid-derived molecule that inhibits cancer cell growth and angiogenesis by inducing apoptosis and binds to small heterodimer partner nuclear receptor: Effects of modifying its carboxylate group on apoptosis, proliferation, and
Dawson, Marcia I.,Xia, Zebin,Liu, Gang,Fontana, Joseph A.,Farhana, Lulu,Patel, Bhamik B.,Arumugarajah, Sankari,Bhuiyan, Mohammad,Zhang, Xiao-Kun,Han, Young-Hoon,Stallcup, William B.,Fukushi, Jun-Ichi,Mustelin, Tomas,Tautz, Lutz,Su, Ying,Harris, Danni L.,Waleh, Nahid,Hobbs, Peter D.,Jong, Ling,Chao, Wan-Ru,Schiff, Leonard J.,Sani, Brahma P.
, p. 2622 - 2639 (2008/02/04)
Apoptotic and antiproliferative activities of small heterodimer partner (SHP) nuclear receptor ligand (E)-4-[3′-(1-adamantyl)-4′- hydroxyphenyl]-3-chlorocinnamic acid (3-Cl-AHPC), which was derived from 6-[3′-(1-adamantyl)-4′-hydroxyphenyl]-2-naphthalenec
