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2,6-Dithia-1,3,5,7-tetraazabicyclo[3.3.1]nonane, 3,7-bis(phenylmethyl)-, 2,2,6,6-tetraoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106013-55-2

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106013-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106013-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,1 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106013-55:
(8*1)+(7*0)+(6*6)+(5*0)+(4*1)+(3*3)+(2*5)+(1*5)=72
72 % 10 = 2
So 106013-55-2 is a valid CAS Registry Number.

106013-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-Dibenzyl-2,6,1,3,5,7-dithiatetraazabicyclo<3.3.1>nonane 2,2,6,6-tetraoxide

1.2 Other means of identification

Product number -
Other names 3,7-Dibenzyl-2,6-dithia-1,3,5,7-tetraaza-bicyclo[3.3.1]nonane 2,2,6,6-tetraoxide

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:106013-55-2 SDS

106013-55-2Downstream Products

106013-55-2Relevant academic research and scientific papers

Intra- and Intermolecular α-Sulfamidoalkylation Reactions

Lee, Chai-Ho,Kohn, Harold

, p. 6098 - 6104 (2007/10/02)

The utility of α-sulfamidoalkylation processes for the generation of sulfamides has been examined.Select aryl-substituted sulfamides were prepared and then treated with acid.Both intra- and intermolecular α-sulfamidoalkylation transformations were observed to proceed in moderate to good yields.The pathways for these reactions are discussed.The generality of these processes has been demonstrated using N,N'-di(aryl-substituted)sulfamides, and the utility of these reactions was examined for the preparation of cyclic sulfamides of novel structure.

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