1059698-08-6 Usage
Description
(R)-1-(benzo[d]thiazol-2-yl)ethanol is a chiral chemical compound with the molecular formula C9H9NOS. It belongs to the class of benzo[d]thiazole derivatives and features a benzene and a thiazole ring in its structure. The presence of a hydroxyl group in this compound suggests potential interactions with biological systems, making it a candidate for various applications in fields such as pharmaceuticals, materials science, and organic synthesis.
Uses
Used in Pharmaceutical Industry:
(R)-1-(benzo[d]thiazol-2-yl)ethanol is used as an active pharmaceutical ingredient for its potential therapeutic properties. Its unique structure allows for specific interactions with biological targets, which can be exploited in the development of new drugs.
Used in Materials Science:
In the materials science field, (R)-1-(benzo[d]thiazol-2-yl)ethanol is used as a component in the synthesis of novel materials with tailored properties. Its structural features can contribute to the development of advanced materials with applications in various industries.
Used in Organic Synthesis:
(R)-1-(benzo[d]thiazol-2-yl)ethanol serves as a key intermediate in organic synthesis, particularly for the production of other benzo[d]thiazole derivatives. These derivatives may have diverse applications, including as intermediates in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1059698-08-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,9,6,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1059698-08:
(9*1)+(8*0)+(7*5)+(6*9)+(5*6)+(4*9)+(3*8)+(2*0)+(1*8)=196
196 % 10 = 6
So 1059698-08-6 is a valid CAS Registry Number.
1059698-08-6Relevant 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.
