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226065-32-3

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226065-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226065-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,0,6 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 226065-32:
(8*2)+(7*2)+(6*6)+(5*0)+(4*6)+(3*5)+(2*3)+(1*2)=113
113 % 10 = 3
So 226065-32-3 is a valid CAS Registry Number.

226065-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-amino-N-(4-cyanophenyl)carbamate

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:226065-32-3 SDS

226065-32-3Relevant articles and documents

Starazo triple switches - synthesis of unsymmetrical 1,3,5-tris(arylazo)benzenes

Heindl, Andreas H.,Wegner, Hermann A.

, p. 22 - 31 (2020)

Multistate switches allow to drastically increase the information storage capacity and complexity of smart materials. In this context, unsymmetrical 1,3,5-tris(arylazo)benzenes - 'starazos' - which merge three photoswitches on one benzene ring, were succe

Synthesis of N-aryl hydrazides by copper-catalyzed coupling of hydrazides with aryl iodides.

Wolter,Klapars,Buchwald

, p. 3803 - 3805 (2007/10/03)

[reaction--see text] A convenient method for intermolecular N-arylation of hydrazides with substituted aryl iodides in the presence of a copper catalyst and Cs(2)CO(3) is reported. The C-N coupling of N-Boc hydrazine with para- and meta-substituted aryl iodides afforded the N-arylated products A, regioselectively. A reversal in regioselectivity is observed for the arylation of benzoic hydrazide with ortho-substituted aryl iodides, providing the N'-arylated products B.

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