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16297-07-7

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16297-07-7 Usage

Uses

2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile may be used in the preparation of 2-anilino-3,5,6-trifluoroisonicotinonitrile.

General Description

2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile is a perfluorinated heteroaromatic compound. 2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile (tetrafluoro-4-cyanopyridine) reacts with 1,3-dicarbonyl systems to yield the corresponding [5,6]-ring fused furo derivatives. 2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile (4-cyanotetrafluoropyridine) reacts with amidines to yield [6,6]-fused pyrimidinopyridine system via nucleophilic substitution at the C-3 position of the pyridine ring followed by intramolecular cyclization onto the pendant cyano group. Reaction of 2,3,5,6-tetrafluoro-4-pyridinecarbonitrile (4-cyanotetrafluoropyridine) with sulfur centred nucleophiles has been reported.

Check Digit Verification of cas no

The CAS Registry Mumber 16297-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,9 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16297-07:
(7*1)+(6*6)+(5*2)+(4*9)+(3*7)+(2*0)+(1*7)=117
117 % 10 = 7
So 16297-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C6F4N2/c7-3-2(1-11)4(8)6(10)12-5(3)9

16297-07-7 Well-known Company Product Price

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  • Aldrich

  • (344591)  2,3,5,6-Tetrafluoro-4-pyridinecarbonitrile  99%

  • 16297-07-7

  • 344591-1G

  • 453.96CNY

  • Detail

16297-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetrafluoropyridine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 2,3,4,5-TETRAFLUOROBENZYLAMINE

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16297-07-7 SDS

16297-07-7Relevant articles and documents

Organocatalyzed Fluoride Metathesis

Mulryan, Daniel,White, Andrew J. P.,Crimmin, Mark R.

supporting information, p. 9351 - 9355 (2020/11/30)

A new organocatalyzed fluoride metathesis reaction between fluoroarenes and carbonyl derivatives is reported. The reaction exchanges fluoride (F-) and alternate nucleophiles (OAc-, OCO2R-, SR-, Cl-, CN-, NCS-). The approach provides a conceptually novel route to manipulate the fluorine content of organic molecules. When the fluorination and defluorination steps are combined into a single catalytic cycle, a byproduct free and 100% atom-efficient reaction can be achieved.

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