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36802-08-1

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36802-08-1 Usage

Molecular structure

Bicyclic ring containing a sulfur and oxygen atom

Chirality

Chiral molecule

Stereochemistry

(3R,4S)

Potential applications

a. Organic synthesis
b. Pharmaceuticals
c. Materials science

Research relevance

a. Study of thiophene chemistry
b. Development of new chemical reactions

Unique structure

Interesting target for further investigation

Potential use

Various fields due to its unique properties and structure

Check Digit Verification of cas no

The CAS Registry Mumber 36802-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,0 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36802-08:
(7*3)+(6*6)+(5*8)+(4*0)+(3*2)+(2*0)+(1*8)=111
111 % 10 = 1
So 36802-08-1 is a valid CAS Registry Number.

36802-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dioxido-(3R,4S)-tetrahydrothiophene-3,4-diol

1.2 Other means of identification

Product number -
Other names 1,1-dioxo-tetrahydro-1λ6-thiophene-3r,4c-diol

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:36802-08-1 SDS

36802-08-1Relevant articles and documents

Oxygen-17 Nuclear Magnetic Resonance Spectral Investigation of 3-Alkoxy-trans-3,4-Disubstituted-Thiolane 1,1-Dioxides and Related Compounds

Sammakia, Tarek H.,Harris, David L.,Evans, Slayton A.

, p. 747 - 752 (2007/10/02)

The (17)O NMR spectra of 3-alkoxythiolane 1,1-dioxides indicate that the sulfonyl oxygens are diastereotopic but their chemical shift differences are essentially independent of the structure of the alkyl group in the alkoxy moiety.Eu(fod)3 enhances the (17)O chemical shift difference between the diastereotopic sulfonyl oxygens in 3-isopropoxythiolane 1,1-dioxide and shifts both oxygens upfield. α,β-Unsaturation deshields the sulfonyl oxygens in both five- and six-membered rings.

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