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9-Thiabicyclo[3.3.1]non-6-en-2-ol is a sulfur-containing organic compound with the molecular formula C6H9OS. It is a heterocyclic compound, specifically a thiabicyclo structure, which features a six-membered ring with a sulfur atom and a five-membered ring fused to it. 9-Thiabicyclo[3.3.1]non-6-en-2-ol is known for its unique chemical properties and potential applications in the synthesis of various pharmaceuticals and agrochemicals. It is characterized by its enolic hydroxyl group, which can participate in various chemical reactions, making it a versatile building block in organic synthesis. The compound's structure and reactivity make it a subject of interest in the field of organic chemistry, particularly for its potential use in the development of new drugs and other chemical products.

6435-91-2

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6435-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6435-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6435-91:
(6*6)+(5*4)+(4*3)+(3*5)+(2*9)+(1*1)=102
102 % 10 = 2
So 6435-91-2 is a valid CAS Registry Number.

6435-91-2SDS

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 9-thiabicyclo[3.3.1]non-2-en-6-ol

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6435-91-2 SDS

6435-91-2Downstream Products

6435-91-2Relevant academic research and scientific papers

PHOTOCHEMICAL AND ASSISTED CLEAVAGES OF HALO-9-THIABICYCLONONANES

McCabe, Peter Heggison,Jenga, Chine Isaac de,Stewart, Angus

, p. 3681 - 3682 (2007/10/02)

A new, high-yield photodehydroiodination of 8 is contrasted with base and silver salt treatments of thiabicyclic halides, which mainly undergo replacements by substitution or elimination-addition.

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