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75732-50-2

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75732-50-2 Usage

General Description

"(2,2-dioxido-1,2-oxathiolan-3-yl)(diphenyl)methanol" is a chemical compound with a complex chemical structure. It contains a 1,2-oxathiolane ring and a diphenylmethanol group. The molecular formula of this compound is C20H18O3S and it has a molecular weight of 346.42 g/mol. The compound is often used in organic synthesis and pharmaceutical research due to its unique structure and potential pharmacological properties. However, further research is needed to fully understand its potential uses 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.

75732-50-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-dioxooxathiolan-3-yl)-diphenylmethanol

1.2 Other means of identification

Product number -
Other names Stannane,(1,3-dihydro-2,2-dioxidobenzo[c]thien-5-yl)trimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75732-50-2 SDS

75732-50-2Relevant articles and documents

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.

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