58692-65-2 Usage
Chemical Family
Alcohols
1-phenyl-1-(2-phenylcyclopropyl)ethanol belongs to the family of alcohols, which are organic compounds with a hydroxyl (-OH) functional group.
Molecular Structure
Phenyl and Cyclopropyl Groups
The compound is composed of a phenyl group (a six-membered aromatic ring with hydrogen atoms) and a cyclopropyl group (a three-membered carbon ring) attached to an ethanol molecule (an alcohol with two carbon atoms).
Usage in Organic Synthesis
Building Block
1-phenyl-1-(2-phenylcyclopropyl)ethanol is often used in organic synthesis and medicinal chemistry as a building block for creating complex molecules, due to its unique structure and reactivity.
Potential Applications
Pharmaceuticals, Fragrances, and Flavors
The compound has potential applications in the development of pharmaceuticals, as well as in the production of fragrances and flavors, thanks to its versatile chemical properties.
Unique Structure
Diverse and Interesting Compounds
The unique structure of 1-phenyl-1-(2-phenylcyclopropyl)ethanol makes it a valuable tool for creating diverse and interesting chemical compounds with potential therapeutic or commercial value.
Check Digit Verification of cas no
The CAS Registry Mumber 58692-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58692-65:
(7*5)+(6*8)+(5*6)+(4*9)+(3*2)+(2*6)+(1*5)=172
172 % 10 = 2
So 58692-65-2 is a valid CAS Registry Number.
58692-65-2Relevant articles and documents
A HIGHLY STEREOSELECTIVE SYNTHESIS OF SUBSTITUTED BUTADIENES AND CONJUGATED POLYENES
Patro, Balaram,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar
, p. 809 - 812 (2007/10/02)
A highly stereoselective synthesis of 1,3-butadienes and its higher enyl analogs has been developed through thermal dehydrative ring opening of cyclopropyl carbinols in dimethylsulphoxide.
