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61653-34-7

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61653-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61653-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,5 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61653-34:
(7*6)+(6*1)+(5*6)+(4*5)+(3*3)+(2*3)+(1*4)=117
117 % 10 = 7
So 61653-34-7 is a valid CAS Registry Number.

61653-34-7SDS

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 bis(2-ethylphenyl)diazene

1.2 Other means of identification

Product number -
Other names 2.2'-Diaethyl-azobenzol

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:61653-34-7 SDS

61653-34-7Relevant articles and documents

Azo synthesis meets molecular iodine catalysis

Rowshanpour, Rozhin,Dudding, Travis

, p. 7251 - 7256 (2021/02/26)

A metal-free synthetic protocol for azo compound formation by the direct oxidation of hydrazine HN-NH bonds to azo group functionality catalyzed by molecular iodine is disclosed. The strengths of this reactivity include rapid reaction times, low catalyst loadings, use of ambient dioxygen as a stoichiometric oxidant, and ease of experimental set-up and azo product isolation. Mechanistic studies and density functional theory computations offering insight into this reactivity, as well as the events leading to azo group formation are presented. Collectively, this study expands the potential of main-group element iodine as an inexpensive catalyst, while delivering a useful transformation for forming azo compounds.

Catalytic Nitrene Homocoupling by an Iron(II) Bis(alkoxide) Complex: Bulking Up the Alkoxide Enables a Wider Range of Substrates and Provides Insight into the Reaction Mechanism

Yousif, Maryam,Wannipurage, Duleeka,Huizenga, Caleb D.,Washnock-Schmid, Elizabeth,Peraino, Nicholas J.,Ozarowski, Andrew,Stoian, Sebastian A.,Lord, Richard L.,Groysman, Stanislav

supporting information, p. 9425 - 9438 (2018/08/17)

The reaction of HOR′ (OR′ = di-t-butyl-(3,5-diphenylphenyl)methoxide) with an iron(II) amide precursor forms the iron(II) bis(alkoxide) complex Fe(OR′)2(THF)2 (2). 2 (5-10 mol %) serves as a catalyst for the conversion of aryl azides

POLYMER SUPPORTED REAGENTS AND METHODS OR REDUCING AROMATIC NITRO COMPOUNDS BY USING THE SAME

-

Paragraph 0117, (2013/10/07)

The present invention relates to a polymer supported reagent comprising a novel crosslinked mesoporous polymer, enabling a simple and easy production of an azoxy compound or an azo compound from an aromatic nitro compound, and a method of selectively reducing an aromatic nitro compound by using the same. The polymer supported reagent comprises a certain acrylamide mesoporous crosslinked polymer.

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