155499-25-5 Usage
Uses
Used in Pharmaceutical Industry:
1,3-Dithiolane-2-acetic acid, 2-[1-(3-hydroxyphenyl)-2-(phenylmethoxy)ethyl]-, ethyl ester, (S)is used as a building block in the synthesis of biologically active molecules for the development of new pharmaceuticals. Its unique structure and functional groups may contribute to the creation of innovative medications that address various medical conditions.
Further research is essential to fully understand the potential applications and effects of this chemical compound, as its current uses are primarily speculative based on its chemical properties and structure. As the pharmaceutical industry continues to explore novel compounds for drug development, 1,3-Dithiolane-2-acetic acid, 2-[1-(3-hydroxyphenyl)-2-(phenylmethoxy)ethyl]-, ethyl ester, (S)may prove to be a valuable asset in the discovery and synthesis of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 155499-25-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,4,9 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 155499-25:
(8*1)+(7*5)+(6*5)+(5*4)+(4*9)+(3*9)+(2*2)+(1*5)=165
165 % 10 = 5
So 155499-25-5 is a valid CAS Registry Number.
155499-25-5Relevant academic research and scientific papers
Enantio- and diastereoselective synthesis of the AB ring system of aklavinone by coupling a chemoenzymatic procedure with organometal chemistry
Banfi, Luca,Guanti, Giuseppe,Riva, Renata
, p. 13493 - 13512 (2007/10/03)
Two different approaches were investigated in order to prepare the title compound 2; best results were obtained when the tandem reduction/intramolecular hydroxyalkylation of the appropriate 5-alkoxy-(3-hydroxyphenyl)pentanoate was performed on an ester of chemoenzymatic origin, already bearing the two chiral centers present in 2 with the correct relative and absolute stereochemistry.
Chemoenzymatic approach to the AB ring system of Aklavinone
Guanti, Giuseppe,Banfi, Luca,Brusco, Stefano,Riva, Renata
, p. 8549 - 8552 (2007/10/02)
Both enantiomers of compound 3, a possible intermediate for the AB ring system 2 of Aklavinone 1, were obtained in optically active form from diol 7. Key steps were the preparation of both enantiomers of monoacetate 8d, via enzymatic reactions that utiliz
