96965-14-9 Usage
Uses
Used in Chemical Synthesis:
(S)-2-Acetoxypropanethioamide is used as a reagent in chemical synthesis for its ability to form various types of organic compounds due to its acetoxy and thio functionalities.
Used in Pharmaceutical Synthesis:
(S)-2-Acetoxypropanethioamide is used as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs for the treatment of various diseases.
Used in Medical Research:
(S)-2-Acetoxypropanethioamide is used as a potential compound in cancer research, exploring its applications in the development of novel treatments for cancer.
Used in Organic Synthesis Industry:
(S)-2-Acetoxypropanethioamide is used as a versatile reagent for the formation of a wide range of organic compounds, enhancing the capabilities of the industry in creating new chemical entities.
Used in Pharmaceutical Industry:
(S)-2-Acetoxypropanethioamide is used as a key building block in the development of new pharmaceuticals, playing a crucial role in the advancement of drug discovery and treatment options for various diseases.
Used in Medical Field:
(S)-2-Acetoxypropanethioamide is used in the medical field for its potential applications in the development of drugs for the treatment of various diseases, including its role in cancer research and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 96965-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,6 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96965-14:
(7*9)+(6*6)+(5*9)+(4*6)+(3*5)+(2*1)+(1*4)=189
189 % 10 = 9
So 96965-14-9 is a valid CAS Registry Number.
96965-14-9Relevant articles and documents
A total synthesis of (+)-bacillamide B
Bray, Christopher D.,Olasoji, Joy
, p. 599 - 601 (2010)
A total synthesis of the halophile-derived natural product (+)-bacillamide B is described. The route relies upon a Hantzsch synthesis of ethyl (S)-2-acetoxyethylthiazole-4-carboxylate followed by a dipyridyl disulfide-mediated coupling between the corresponding carboxylic acid and tryptamine. This synthesis has unambiguously demonstrated that in contrast to the previous tentative stereochemical assignments the stereochemistry of the alcohol at C15 of the title compound has S-configuration. Georg Thieme Verlag Stuttgart · New York.
What is the structure of the patellamides?
Schmidt,Utz,Gleich
, p. 4367 - 4370 (2007/10/02)
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