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70891-88-2

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70891-88-2 Usage

Chemical structure

1-[phenyl(phenylsulfinyl)methyl]triaza-1,2-dien-2-ium is a compound with a central triaza-dien-2-ium core and a phenyl(phenylsulfinyl)methyl substituent.

Charge

The compound has a positively charged nitrogen atom.

Reactivity

The presence of the sulfinyl group adds a high degree of reactivity to the compound.

Potential applications

Due to its unique structure and reactivity, the chemical may have potential applications in organic synthesis, medicinal chemistry, and material science.

Research status

Further research is needed to fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 70891-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,9 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70891-88:
(7*7)+(6*0)+(5*8)+(4*9)+(3*1)+(2*8)+(1*8)=152
152 % 10 = 2
So 70891-88-2 is a valid CAS Registry Number.

70891-88-2SDS

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 [azido(benzenesulfinyl)methyl]benzene

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:70891-88-2 SDS

70891-88-2Relevant articles and documents

Thermolysis of α-Azido Sulfides, Sulfoxides, and Sulfones: Dependence of Mechanism on Oxidation State of Sulfur

Jarvis, Bruce B.,Nicholas, Paul E.,Midiwo, Jacob O.

, p. 3878 - 3882 (1981)

Thermolyses of α-azidobenzyl phenyl sulfide (1), sulfoxide (3), and sulfone (2) proceed at markedly different rates.Sulfone 2 requires the highest temperature (> 150 deg C), whereas sulfide 1 loses nitrogen at 120 deg C with neighboring group participation by the sulfur atom to produce N-benzylidenebenzenesulfenamide 4 in 75percent yield.Sulfoxide 3 readily decomposes at 70 deg C through a radical-pair intermediate, which gives rise to a CIDNP effect in the reaction products.Kinetic data are presented supporting the suggested reaction mechanisms.

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