1373756-63-8 Usage
Uses
Used in Organic Synthesis:
(3S,6S)-6-tert-butyldiphenylsilyloxyhept-1-en-3-ol is used as a reagent in various chemical reactions for organic synthesis. Its unique structure allows it to participate in a wide range of reactions, making it a valuable tool for chemists.
Used in Medicinal and Pharmaceutical Chemistry:
In the field of medicinal and pharmaceutical chemistry, (3S,6S)-6-tert-butyldiphenylsilyloxyhept-1-en-3-ol is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its specific stereochemistry and functional groups enable it to be incorporated into complex molecular structures, contributing to the development of new drugs and therapies.
Used in the Development of New Materials and Compounds:
(3S,6S)-6-tert-butyldiphenylsilyloxyhept-1-en-3-ol is also utilized in the development of new materials and compounds. Its unique properties and reactivity make it a promising candidate for creating innovative materials with potential applications in various industries.
Despite its complex name and structure, (3S,6S)-6-tert-butyldiphenylsilyloxyhept-1-en-3-ol plays a significant role in the advancement of chemical research and innovation, contributing to the development of new products and technologies across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1373756-63-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,7,5 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1373756-63:
(9*1)+(8*3)+(7*7)+(6*3)+(5*7)+(4*5)+(3*6)+(2*6)+(1*3)=188
188 % 10 = 8
So 1373756-63-8 is a valid CAS Registry Number.
1373756-63-8Relevant academic research and scientific papers
An Enantioselective Synthesis of (5 S,6 R,11 S,14 R)-Acremodiol
Dey, Papiya,Chatterjee, Sucheta,Gamre, Sunita S.,Chattopadhyay, Subrata,Sharma, Anubha
, p. 5231 - 5237 (2017/11/28)
An expeditious synthesis of the (5 S,6 R,11 S,14 R)-isomer of acremodiol was developed via a convergent route. One of the required building blocks was synthesized earlier via two sequential lipase-catalyzed secondary carbinol acetylations. The other unit
A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: Application to asymmetric synthesis of decarestrictine L, pyrenophorol, and stagonolide e
Chatterjee, Sucheta,Ghadigaonkar, Sneha,Sur, Payel,Sharma, Anubha,Chattopadhyay, Subrata
, p. 8067 - 8076 (2015/03/18)
The stereomers of hept-6-ene-2,5-diol derivatives were conceived as useful chiral intermediates and were synthesized starting from sulcatol using two lipase-catalyzed acylation reactions as the key steps. The versatility of the intermediates was demonstrated by converting them to the titled tetrahydropyran, macrolide, and macrodiolide compounds using standard synthetic protocols.
Total synthesis of (-)-pyrenophorol
Yadav, Jhillu S.,Reddy, Ganapuram Madhusudhan,Rao, Tenneti Srinivasa,Reddy, Basi V. Subba,Al Khazim Al Ghamdi, Ahmad
, p. 783 - 787 (2012/04/10)
An efficient synthetic route has been developed for the synthesis of (-)-pyrenophorol employing Sharpless asymmetric epoxidation, olefin cross-metathesis, and intermolecular Mitsunobu cyclization. Georg Thieme Verlag Stuttgart · New York.
