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4,4'-azopyridine N,N'-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58165-83-6

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58165-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58165-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,6 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58165-83:
(7*5)+(6*8)+(5*1)+(4*6)+(3*5)+(2*8)+(1*3)=146
146 % 10 = 6
So 58165-83-6 is a valid CAS Registry Number.

58165-83-6SDS

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 trans-4,4'-azopyridine dioxide

1.2 Other means of identification

Product number -
Other names trans-[4,4']azopyridine-1,1'-dioxide

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:58165-83-6 SDS

58165-83-6Downstream Products

58165-83-6Relevant academic research and scientific papers

Comparative study of the photochemistry of the azidopyridine 1-oxides

Crabtree, Kyle N.,Hostetler, Katherine J.,Munsch, Tamara E.,Neuhaus, Patrik,Lahti, Paul M.,Sander, Wolfram,Poole, James S.

, p. 3441 - 3451 (2008/09/20)

(Chemical Equation Presented) The photochemistry of azidopyridine 1-oxides was studied using an array of glass and matrix isolation techniques. As with room temperature, the photochemistry of 4-azidopyridine 1-oxide is dominated by triplet nitrene chemistry. However, in the case of the 3-azide, matrix photolysis indicates the formation of diazabicyclo[4.1.0]hepta-2,4,6-triene N-oxide and diazacycloheptatetraene N-oxide intermediates as well as triplet nitrene.

REDUCTION OF AROMATIC NITRO GROUPS WITH HEXAMETHYLDISILANE1): REACTIONS WITH HEXAMETHYLDISILANE AND FLUORIDE ION-II2).

Vorbrueggen, Helmut,Krolikiewicz, Konrad

, p. 1259 - 1262 (2007/10/02)

Reduction of aromatic nitro compounds with hexamethyldisilane and fluoride ion in THF at 24 deg C gives the corresponding azo- and azoxy-compounds in high yields.Hexamethyldisilane converts commercial tetrabutylammoniumfluoride-dihydrate into a highly reactive catalyst.

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