222609-67-8 Usage
Description
(S)-1-(thiophen-3-yl)ethan-1-ol, also known as (3-thien-1-yl)ethan-1-ol, is a chemical compound characterized by its molecular formula C6H8OS. This colorless liquid with a strong odor is recognized for its diverse industrial and research applications, making it a versatile compound in the chemical industry.
Uses
Used in Organic Synthesis:
(S)-1-(thiophen-3-yl)ethan-1-ol is utilized as a fundamental building block in organic synthesis, playing a crucial role in the creation of various complex molecules. Its unique structure allows it to be a valuable component in the development of pharmaceuticals, agrochemicals, and other fine chemicals, contributing to the advancement of these industries.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (S)-1-(thiophen-3-yl)ethan-1-ol is used as a key intermediate in the synthesis of numerous drugs. Its incorporation into drug molecules can enhance their efficacy and selectivity, leading to improved treatment options for various medical conditions.
Used in Agrochemicals:
(S)-1-(thiophen-3-yl)ethan-1-ol also finds application in the agrochemical sector, where it is employed in the synthesis of pesticides and other agricultural chemicals. Its use in this industry helps to develop more effective and targeted products for crop protection and management.
Used as a Solvent:
(S)-1-(thiophen-3-yl)ethan-1-ol serves as a solvent in various chemical processes due to its ability to dissolve a wide range of substances. This property makes it an indispensable component in numerous industrial applications, facilitating smoother and more efficient chemical reactions.
Used in Fragrance Industry:
In the fragrance industry, (S)-1-(thiophen-3-yl)ethan-1-ol is used as an ingredient in perfumes and personal care products. Its strong odor adds a unique and distinct scent to these products, enhancing their appeal and marketability.
Used as a Chiral Auxiliary:
Furthermore, (S)-1-(thiophen-3-yl)ethan-1-ol has potential applications as a chiral auxiliary in asymmetric synthesis. Its chirality allows it to be used in the development of enantiomerically pure compounds, which are essential in various pharmaceutical and chemical applications where stereochemistry plays a critical role.
Check Digit Verification of cas no
The CAS Registry Mumber 222609-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,6,0 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 222609-67:
(8*2)+(7*2)+(6*2)+(5*6)+(4*0)+(3*9)+(2*6)+(1*7)=118
118 % 10 = 8
So 222609-67-8 is a valid CAS Registry Number.
222609-67-8Relevant 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.
