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2-(3-azabicyclo[3.2.2]non-3-yldisulfanyl)-1,3-benzothiazole is a complex organic compound with the molecular formula C13H16N2S3. It features a benzothiazole ring, which is a fused ring system consisting of a benzene ring and a thiazole ring. The compound is characterized by the presence of a disulfanyl group (-S-S-) attached to the 3-azabicyclo[3.2.2]nonane moiety, which is a nitrogen-containing cyclic structure. This specific arrangement of atoms and functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The compound's structure and properties make it a subject of interest for researchers studying the synthesis and reactivity of complex organic molecules.

2939-53-9

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2939-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2939-53-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2939-53:
(6*2)+(5*9)+(4*3)+(3*9)+(2*5)+(1*3)=109
109 % 10 = 9
So 2939-53-9 is a valid CAS Registry Number.

2939-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-azabicyclo[3.2.2]nonan-3-yldisulfanyl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 3-(2-Benzothiazolyldithio)-3-aza-bicyclo<3.2.2.>nonan

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

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More Details:2939-53-9 SDS

2939-53-9Upstream product

2939-53-9Downstream Products

2939-53-9Relevant academic research and scientific papers

Base catalysis of azolesulfenamides and sulfur to aminodithioazoles

-

, (2008/06/13)

The reaction of azolesulfenamides with sulfur to form aminodithioazoles is promoted by catalytic quantities of certain bases.

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