153035-65-5 Usage
Description
(+)-(R)-1-(thiophen-3-yl)ethanol, also known as (+)-3-Thienylethanol or 3-Thienyl ethanol, is a chiral compound with a molecular formula C6H6OS. It is characterized by its distinct sweet, floral odor and is commonly used as a chiral building block in the synthesis of pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
(+)-(R)-1-(thiophen-3-yl)ethanol is used as a chiral building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique properties make it a valuable component in the development of new drugs.
Used in Fragrance and Flavor Industry:
(+)-(R)-1-(thiophen-3-yl)ethanol is used as a fragrance and flavor ingredient due to its distinct sweet, floral odor. It adds a pleasant scent and taste to various products in this industry.
Used in Antimicrobial and Insecticidal Applications:
(+)-(R)-1-(thiophen-3-yl)ethanol is known for its antimicrobial and insecticidal properties, making it a potential candidate for use in the development of new treatments and products to combat infections and pests.
Used in Medical Research:
(+)-(R)-1-(thiophen-3-yl)ethanol has been studied for its potential role in the treatment of various medical conditions, including cancer and infectious diseases. Its unique properties and potential applications make it a promising compound for further research and development in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 153035-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,3 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153035-65:
(8*1)+(7*5)+(6*3)+(5*0)+(4*3)+(3*5)+(2*6)+(1*5)=105
105 % 10 = 5
So 153035-65-5 is a valid CAS Registry Number.
153035-65-5Relevant articles and documents
Kinetic resolution of racemic 1-heteroarylalkanols by asymmetric esterification using diphenylacetic acid with pivalic anhydride and a chiral acyl-transfer catalyst
Shiina, Isamu,Ono, Keisuke,Nakata, Kenya
supporting information; experimental part, p. 147 - 149 (2011/04/14)
A variety of optically active 1-heteroarylalkanols and their esters, which include heteroaromatic moieties, such as 2-furyl, 2-thienyl, 3-thienyl, 2-thiazoyl, 2-benzothiazoyl, and 2-benzoxazoyl groups, are efficiently produced by a novel asymmetric esterification. The transition states that form the desired (R)- esters from the (R)-1-heteroarylalkanols are determined by DFT calculations, and the structural features of these transition states are systematically discussed.
