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16297-09-9

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16297-09-9 Usage

Physical state

Yellow liquid at room temperature

Uses

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals; production of crop protection products; building block in the development of new materials

Importance

Versatile chemical, crucial in the development of various chemical products, plays a significant role in the field of organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 16297-09-9 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 16297-09:
(7*1)+(6*6)+(5*2)+(4*9)+(3*7)+(2*0)+(1*9)=119
119 % 10 = 9
So 16297-09-9 is a valid CAS Registry Number.

16297-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names tetrafluoro-pyridine-4-carbaldehyde

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:16297-09-9 SDS

16297-09-9Relevant articles and documents

Chambers, R. D.,Heaton, C. A.,Musgrave, W. K. R.,Chadwick, L.

, p. 1700 - 1703 (1969)

Synthesis of difluorinated pyridinecarboxaldehyde via electrophilic fluorination

Ko, Yoon-Joo,Park, Kyung-Bae,Shim, Seung-Bo,Shin, Jung-Hyu

, p. 755 - 759 (2008/03/28)

An efficient synthesis of novel 3,5-difluoropyridine-4-carboxaldehyde using N-fluoro-benzenesulfonimide (NSFi) is described. Difluorination was achieved through the reaction of 3,5-dihalo-1,3-dioxolane pyridine with n-butyllithium followed by N-fluorobenzenesulfonimide at -120 °C in good to high yields. Maintaining the low temperature during the transmetallation was found to be critical for the selective formation of the difluoro-susbstitution over the monofluoro one.

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