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1-Triazene, 3,3-dimethyl-1-[(4-methylphenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25286-68-4

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25286-68-4 Usage

Usage

Reagent in organic synthesis and potential applications in pharmaceutical industry

Contains a triazene group

Ability to release nitrogen gas when exposed to certain stimuli

Contains a sulfonyl group

Contributes to the compound's reactivity and potential biological activity

Importance

Diverse applications in synthetic chemistry and pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 25286-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,8 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25286-68:
(7*2)+(6*5)+(5*2)+(4*8)+(3*6)+(2*6)+(1*8)=124
124 % 10 = 4
So 25286-68-4 is a valid CAS Registry Number.

25286-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-Dimethyl-1-(4-toluolsulfonyl)-triazen

1.2 Other means of identification

Product number -
Other names 3,3-Dimethyl-1-tosyl-triazen

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:25286-68-4 SDS

25286-68-4Relevant academic research and scientific papers

Nitrosations with hydrazine derivatives: Synthesis of N4-arenesulfinylsemicarbazides and N5-arenesulfinyl-N1-aminobiuretes from arenesulfinylisocyanates and N,N-disubstituted hydrazines

Hanefeld,Landwehr

, p. 344 - 351 (2007/10/02)

Arenesulfinyl-isocyanates 5 prepared in situ from arenesulfinyl chlorides 4 and silver cyanate react with N,N-disubstituted hydrazines to mixtures of N4-arenesulfinylsemicarbazides 6 as main components and N5-arenesulfinyl-N1/s

Nitrosations with hydrazine derivatives. Novel synthesis of arylsulfonyltriazenes by nitrosation of N4-arylsulfonylsemicarbazides

Hanefeld,Hartmann

, p. 672 - 675 (2007/10/02)

N1-disubstituted N4-arenesulfonylsemicarbazides 3 are prepared by hydrazinolysis of the arenesulfonylurethanes 2, which result from arenesulfonamides and chloroformic acid ester. Under nitrosating conditions 3 are mainly transformed into the sulfonyltriazenes 4.

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