77542-06-4 Usage
Uses
Used in Pharmaceutical Research:
1-[4-(2-DIMETHYLAMINO-ETHOXY)PHENYL]-1,2-DIPHENYL-1-BUTANOL is used as a potential drug candidate for various medical conditions due to its unique structure and properties. It is particularly considered for the treatment of cancer and cardiovascular diseases, where its pharmacological effects and potential therapeutic applications are being studied and evaluated.
Used in Cancer Treatment Research:
In the field of cancer treatment, 1-[4-(2-DIMETHYLAMINO-ETHOXY)PHENYL]-1,2-DIPHENYL-1-BUTANOL is used as a potential therapeutic agent. Its specific structure allows researchers to investigate its effects on different types of cancer and explore its potential to contribute to cancer treatment strategies.
Used in Cardiovascular Disease Research:
For cardiovascular diseases, 1-[4-(2-DIMETHYLAMINO-ETHOXY)PHENYL]-1,2-DIPHENYL-1-BUTANOL is used as a compound of interest in research. Its properties are being examined to understand how it may interact with biological systems and potentially offer benefits in the treatment or management of cardiovascular conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 77542-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,4 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77542-06:
(7*7)+(6*7)+(5*5)+(4*4)+(3*2)+(2*0)+(1*6)=144
144 % 10 = 4
So 77542-06-4 is a valid CAS Registry Number.
77542-06-4Relevant academic research and scientific papers
Stereoselective Olefin Formation from the Dehydration of 1-(p-Alkoxyphenyl)-1,2-diphenylbutan-1-ols: Application to the Synthesis of Tamoxifen
McCague, Raymond
, p. 1011 - 1016 (2007/10/02)
Acid-catalysed dehydration of either diastereoisomer of a 1-(p-alkoxyphenyl)-1,2-diphenylbutan-1-ol gives mainly the Z isomer of the but-1-ene via a common carbenium ion intermediate that can be regenerated by protonation of the (Z)- or (E)-butene with fluorosulphonic acid.Highly stereoselective syn eliminations were achieved by treatment of the butan-1-ols with base and carbon disulphide but dehydrations using N,N,N-triethylammonio-N'-methoxycarbonylsulphamidate proceeded mainly via a carbenium ion.Aspects of the stereoselectivity of the reactions are discussed.The methods can be applied to give simple stereoselective syntheses of the anti-cancer drug tamoxifen.
