4665-63-8 Usage
Uses
Used in Chemical Synthesis:
2-(2-Benzothiazolylthio)ethanol is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure, which includes a benzothiazole ring, sulfur, nitrogen, and an ethanol chain, makes it a valuable building block in the development of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
2-(2-Benzothiazolylthio)ethanol is used as a starting material for the development of new pharmaceutical compounds. Its chemical properties, such as the presence of a benzothiazole ring and an alcohol functional group, can be exploited to create novel drug candidates with potential therapeutic applications.
Used in Material Science:
2-(2-Benzothiazolylthio)ethanol is used as a component in the development of new materials with specific properties. Its chemical structure can contribute to the creation of materials with unique characteristics, such as improved stability, reactivity, or other desirable traits.
Safety Precautions:
Due to the limited safety information available for 2-(2-Benzothiazolylthio)ethanol, it is crucial to handle 2-(2-BENZOTHIAZOLYLTHIO)ETHANOL with appropriate safety measures. It is suggested that it might be harmful if swallowed, inhaled, or comes into contact with skin. Therefore, it is essential to follow standard safety protocols, such as wearing protective clothing, using gloves, and working in a well-ventilated area, to minimize the risk of exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 4665-63-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4665-63:
(6*4)+(5*6)+(4*6)+(3*5)+(2*6)+(1*3)=108
108 % 10 = 8
So 4665-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NOS2/c11-5-6-12-9-10-7-3-1-2-4-8(7)13-9/h1-4,11H,5-6H2
4665-63-8Relevant academic research and scientific papers
Enantioselective total syntheses of (+)-gallocatechin, (-)- epigallocatechin, and 8-C-ascorbyl-(-)-epigallocatechin
Lin, Guang,Chang, Le,Liu, Yongxiang,Xiang, Zheng,Chen, Jiahua,Yang, Zhen
supporting information, p. 700 - 704 (2013/05/09)
Reading the tea leaves: The enatioselective total syntheses of 8-C-ascorbyl-(-)-epigallocatechin was accomplished by CuII-mediated oxidative coupling of ascorbic acid and (-)-epigallocatechin as a key step. Also, the asymmetric total syntheses of tea-leaf extracts (+)-gallocatechin and (-)-epigallocatechin were achieved by Au-catalyzed intramolecular cycliarylation of the precursor epoxide and Sharpless dihydroxylation. Copyright
HYDROXYALKYL DERIVATIVES OF BIOLOGICALLY ACTIVE COMPOUNDS
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Page/Page column 13, (2010/02/14)
Hydroxyalkyl derivatives of biologically active compounds represented by the formula VII wherein R2 = H, CI-12 alkyl, C6-12 aryl, or -OH and D = Biologically active agent having functional groups such as Formula (a) epoxy or aziridine and Z' = Formula (b) L= spacer comprising (un)substituted alkyl, hydroxyalkyl or alkoxy alkyl with the condition that the carbon chain length contains 2 to 6 carbon atoms when Z' = Formula (c) and pharmaceutically acceptable acid addition salts and enantiomers thereof Also process for the synthesis of compounds of the Formula VII and pharmaceutically acceptable acid addition salts and enantiomers thereof comprising condensation of the biologically active agents having functional groups such as Formula (d) epoxy or azifidine with substituted alkyl derivatives under alkaline conditions, at 20 - 80°C, in an organic solvent.
