75732-50-2 Usage
Uses
Used in Organic Synthesis:
(2,2-dioxido-1,2-oxathiolan-3-yl)(diphenyl)methanol serves as a valuable intermediate in organic synthesis, particularly for the creation of complex molecular structures. Its unique 1,2-oxathiolane ring and diphenylmethanol group provide a versatile platform for the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2,2-dioxido-1,2-oxathiolan-3-yl)(diphenyl)methanol is utilized for its potential pharmacological properties. Its distinctive structure may contribute to the discovery of new drugs, although ongoing research is necessary to fully understand its therapeutic applications and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 75732-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,3 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75732-50:
(7*7)+(6*5)+(5*7)+(4*3)+(3*2)+(2*5)+(1*0)=142
142 % 10 = 2
So 75732-50-2 is a valid CAS Registry Number.
75732-50-2Relevant academic research and scientific papers
Lithium aluminum hydride-aluminum hydride reduction of sultones
Smith, Michael B.,Wolinsky, Joseph
, p. 101 - 106 (2007/10/02)
Lithium aluminum hydride-aluminum hydride reduction of secondary and tertiary (C-O) substituted γ-sultones or α-alkyl-β'-hydroxy γ-sultones yields mercapto alcohols and mercapto diols, respectively, in fair to good yield.These products result from S-O cleavage of the sultone ring.Primary sultones and α-dialkyl-β'-hydroxy γ-sultones give predominantly C-O cleavage to form sulfonic acid derivatives. β-Sultones are much less reactive toward the mixed hydride, and refluxing in dioxane is required for their reduction.
