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22237-37-2

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22237-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22237-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,3 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22237-37:
(7*2)+(6*2)+(5*2)+(4*3)+(3*7)+(2*3)+(1*7)=82
82 % 10 = 2
So 22237-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12Cl2N2/c1-9-3-5-11(7-13(9)15)17-18-12-6-4-10(2)14(16)8-12/h3-8H,1-2H3/b18-17+

22237-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3.3'-Dichlor-4.4'-dimethyl-azobenzol

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:22237-37-2 SDS

22237-37-2Upstream product

22237-37-2Downstream Products

22237-37-2Relevant 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.

Chloroazobenzenes: studies on syntheses.

Linke,Bartha,Pramer

, p. 994 - 996 (2007/10/05)

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