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21418-21-3

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21418-21-3 Usage

General Description

2-(Cyanoamino)pyridine is a chemical compound with the formula C6H5N3. It is an organic compound that belongs to the pyridine family and contains a cyanoamino group, which is a cyano group (-CN) and an amino group (-NH2) attached to a pyridine ring. 2-(Cyanoamino)pyridine is used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also a versatile building block for the synthesis of various other compounds due to its unique structure and properties. 2-(Cyanoamino)pyridine has potential applications in the field of medicinal chemistry, as it can serve as a precursor for the synthesis of inhibitors and bioactive compounds. Additionally, it may be used as a ligand in coordination chemistry due to its ability to coordinate with metal ions.

Check Digit Verification of cas no

The CAS Registry Mumber 21418-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,1 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21418-21:
(7*2)+(6*1)+(5*4)+(4*1)+(3*8)+(2*2)+(1*1)=73
73 % 10 = 3
So 21418-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5N3/c7-5-9-6-3-1-2-4-8-6/h1-4H,(H,8,9)

21418-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name pyridin-2-ylcyanamide

1.2 Other means of identification

Product number -
Other names N-(pyridin-2-yl)cyanamide

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:21418-21-3 SDS

21418-21-3Relevant articles and documents

A highly regioselective reaction of N-fluoropyridinium salts with stabilized sulfur, oxygen, and nitrogen nucleophiles: A convenient route to 2-substituted pyridines

Kiselyov,Strekowski

, p. 1361 - 1364 (2007/10/02)

2-Substituted pyridines are efficiently obtained by the reactions of N- fluoropyridinium tetrafluoroborate or triflate with anions derived from benzenethiols, phenols, azoles, cyanamide, and with azide anion. The results are consistent with a nucleophile addition at the position 2 of the N- fluoropyridinium cation as the major reaction pathway.

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