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4663-97-2

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4663-97-2 Usage

Uses

2,6-Pyridinedicarboxamide may be used in the preparation of new molecular turnstiles based on Sn-porphyrin derivatives.

General Description

2,6-Pyridinedicarboxamide is an excellent tridentate ligand for transition metals (Cu2+, Ni2+).

Check Digit Verification of cas no

The CAS Registry Mumber 4663-97-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4663-97:
(6*4)+(5*6)+(4*6)+(3*3)+(2*9)+(1*7)=112
112 % 10 = 2
So 4663-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O2/c8-6(11)4-2-1-3-5(10-4)7(9)12/h1-3H,(H2,8,11)(H2,9,12)

4663-97-2 Well-known Company Product Price

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  • Aldrich

  • (464902)  2,6-Pyridinedicarboxamide  97%

  • 4663-97-2

  • 464902-10G

  • 1,560.78CNY

  • Detail

4663-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Pyridine-2,6-dicarboxamide

1.2 Other means of identification

Product number -
Other names 2,6-Pyridinedicarboxamide

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:4663-97-2 SDS

4663-97-2Upstream product

4663-97-2Relevant articles and documents

Catalytic hydration of cyanopyridines using nickel(0)

Crisóstomo, Carmela,Crestani, Marco G.,García, Juventino J.

experimental part, p. 1092 - 1096 (2010/06/15)

The homogeneous catalytic hydration of 2-, 3- and 4-cyanopyridines using 0.5 mol% of [(dippe)Ni(μ-H)]2 as catalyst precursor was achieved under heating. In the case of 4-cyanopyridine, production of isonicotinamide was observed at temperatures in the range of 80-120 °C. Heating to 180 °C resulted in formation of isonicotinic acid. In the case of 2- and 3-cyanopyridines the quantitative formation of their corresponding amides was achieved at 100 °C. The catalytic hydration of 2,6-dicyanopyridine was also undertaken in this work, in its case resulting in the synthesis of the mixed cyano/amide product, 2-cyanopyridine-6-carboxamide, at short reaction times.

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