Description

The pyridine compound is one of the most widely developed varieties of heterocyclic compounds. 3-Fluoropicolinonitrile is one of the pyridine compounds and is also an excellent intermediate for an important fine chemical raw material. It Harmful if swallowed, also causes skin irritation and causes serious eye irritation. So be careful when you use it.

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3-Fluoropicolinonitrile (97509-75-6) Specifications

CAS	97509-75-6
CAS Min %	95.0
CAS Max %	100.0
MDL Number	MFCD06797501
InChI Key	VZFPSCNTFBJZHB-UHFFFAOYSA-N
Chemical Name or Material	3-Fluoropicolinonitrile
Infrared Spectrum	Authentic
Physical Form	Powder or Chunks
Packaging	Glass bottle
Molecular Formula	C6H3FN2
Molecular Weight (g/mol)	122.102
SMILES	C1=CC(=C(N=C1)C#N)F
Color	White
Melting Point	27° to 30°C
Assay	≥97%

3-Fluoropicolinonitrile (97509-75-6) Safety and Handling

(97509-75-6) Hazard description:

• Harmful if swallowed.
• Causes skin irritation.
• Causes serious eye irritation.

3-Fluoropicolinonitrile Precautionary statement:

Wear protective gloves/clothing.

IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

WARNING: The information provided on this web site was developed in compliance with European Union (EU) regulations and is correct to the best of our knowledge, information and belief at the date of its publication. The information given is designed only as a guide for safe handling and use. It is not to be considered as either a warranty or quality specification.

3-Fluoropicolinonitrile (97509-75-6) Articles

Arylboronic Acids

Aldrich is pleased to present its complete selection of arylboronic acids, the building blocks of the Suzuki coupling experiment…

Aldrich ChemFiles 2001,

Boronic Acids

Most boronic acids readily undergo dehydration reactions to give a cyclic (trimer) anhydride…

Aldrich ChemFiles 2007,

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