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14213-02-6

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14213-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14213-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,1 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14213-02:
(7*1)+(6*4)+(5*2)+(4*1)+(3*3)+(2*0)+(1*2)=56
56 % 10 = 6
So 14213-02-6 is a valid CAS Registry Number.

14213-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-azidoquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,3-azido

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:14213-02-6 SDS

14213-02-6Relevant articles and documents

Synthesis, characterization and antibacterial activity of the thioether linked 1,2,3-triazoles

Kaushik, Chander P.,Sangwan, Jyoti

supporting information, p. 3403 - 3415 (2021/09/13)

A green synthetic approach for the expedite construction of thirty six thioether linked 1,2,3-triazoles was carried out using Cellulose supported CuI nanoparticles in water. The structure of synthesized triazoles was explicated by spectroscopic techniques

Aryl Azides as Forgotten Electrophiles in the Van Leusen Reaction: A Multicomponent Transformation Affording 4-Tosyl-1-arylimidazoles

Necardo, Cristiana,Alfano, Antonella Ilenia,Del Grosso, Erika,Pelliccia, Sveva,Galli, Ubaldina,Novellino, Ettore,Meneghetti, Fiorella,Giustiniano, Mariateresa,Tron, Gian Cesare

, p. 16299 - 16307 (2019/12/27)

Considering aryl azides as electrophilic partners for the TosMIC mediated Van Leusen reaction, a novel multicomponent synthesis of 4-tosyl-1-arylimidazoles is reported. In this transformation, two molecules of TosMIC participate in the reaction mechanism

Palladium-catalyzed cross-coupling reaction of azides with isocyanides

Zhang, Zhen,Li, Zongyang,Fu, Bin,Zhang, Zhenhua

supporting information, p. 16312 - 16315 (2015/11/16)

An efficient palladium-catalyzed cross-coupling reaction of azides with isocyanides is developed, providing a general synthetic route to unsymmetric carbodiimides with excellent yields. This method shows a broad substrate scope, including not only aryl azides, but also unactivated benzyl and alkyl azides. Furthermore, from readily available substrates, Pd-catalyzed coupling with a tandem amine insertion cascade to obtain unsymmetric trisubstituted guanidines has been achieved in a one-pot fashion.

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