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372-48-5

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372-48-5 Usage

Description

2-Fluoropyridine is a clear, colorless to light yellow liquid that serves as a versatile building block in the synthesis of various organic compounds, particularly in the pharmaceutical and chemical industries. It is characterized by its fluorine atom at the 2nd position on the pyridine ring, which imparts unique reactivity and properties to the molecule.

Uses

Used in Pharmaceutical Industry:
2-Fluoropyridine is used as a synthetic intermediate for the development of 2,3-disubstituted pyridines. Its ability to undergo metallation at the C-3 position, along with the nucleophilic displacement of the activated fluorine, makes it a valuable precursor in the synthesis of these compounds. This application is particularly relevant in the creation of novel drugs and therapeutic agents.
Used in Chemical Industry:
2-Fluoropyridine is used as a reagent in the chemical industry for the synthesis of aminopyridines. These compounds are important building blocks for the development of various pharmaceuticals, agrochemicals, and other specialty chemicals. The unique reactivity of the fluorine atom in 2-fluoropyridine allows for efficient and selective reactions, leading to the formation of desired products.
Used in Heterocyclic Chemistry:
2-Fluoropyridine is also used in the synthesis of 2-thiophen-2-yl-pyridine by reacting with thiophene. 2-Fluoropyridine is an important intermediate in the preparation of various heterocyclic compounds, which are widely used in the pharmaceutical, agrochemical, and materials science industries. The versatility of 2-fluoropyridine in forming such heterocyclic systems highlights its significance in the field of organic chemistry.

Synthesis

A rare example of fluorodenitration of a heterocyclic system was provided by 2- nitropyridine, which was converted to 2-fluoropyridine.

Check Digit Verification of cas no

The CAS Registry Mumber 372-48-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 372-48:
(5*3)+(4*7)+(3*2)+(2*4)+(1*8)=65
65 % 10 = 5
So 372-48-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H4FN/c6-5-3-1-2-4-7-5/h1-4H

372-48-5 Well-known Company Product Price

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  • TCI America

  • (F0217)  2-Fluoropyridine  >98.0%(GC)

  • 372-48-5

  • 25g

  • 550.00CNY

  • Detail
  • TCI America

  • (F0217)  2-Fluoropyridine  >98.0%(GC)

  • 372-48-5

  • 100g

  • 2,190.00CNY

  • Detail
  • Alfa Aesar

  • (A11627)  2-Fluoropyridine, 99%   

  • 372-48-5

  • 10g

  • 217.0CNY

  • Detail
  • Alfa Aesar

  • (A11627)  2-Fluoropyridine, 99%   

  • 372-48-5

  • 25g

  • 452.0CNY

  • Detail
  • Alfa Aesar

  • (A11627)  2-Fluoropyridine, 99%   

  • 372-48-5

  • 100g

  • 1405.0CNY

  • Detail
  • Alfa Aesar

  • (A11627)  2-Fluoropyridine, 99%   

  • 372-48-5

  • 250g

  • 2885.0CNY

  • Detail
  • Aldrich

  • (F15250)  2-Fluoropyridine  98%

  • 372-48-5

  • F15250-10G

  • 270.27CNY

  • Detail
  • Aldrich

  • (F15250)  2-Fluoropyridine  98%

  • 372-48-5

  • F15250-100G

  • 1,660.23CNY

  • Detail

372-48-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoropyridine

1.2 Other means of identification

Product number -
Other names o-fluoropyridine

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:372-48-5 SDS

372-48-5Relevant articles and documents

Method for pipeline continuous fluorination with fluorine salt as fluorine source

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Paragraph 0056-0061; 0094-0096, (2021/10/27)

The method comprises the following steps: dissolving a fluorine salt in an aqueous polar aprotic solvent as reaction liquid A, dissolving an aryl (heterocyclic) chloride in a polar aprotic solvent as reaction liquid B, and reacting a polar aprotic solvent in the reaction liquid A with a polar aprotic solvent of the reaction liquid B. The reaction medium consisting of the preheated reaction liquid A and the preheated reaction liquid B enters the reaction coil for a fluorination reaction, and the resulting product from the reaction coil is subjected to post-treatment to obtain the product. The method has the characteristics of no need of adding a phase transfer catalyst, continuous production, low production cost and the like.

PROCESS FOR FLUORINATING COMPOUNDS

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Page/Page column 24, (2017/02/28)

Disclosed are mild temperature (e.g., from 0 to 80°C) SNAr fluorinations of a variety of halide and sulfonate substituted aryl and heteroaryl substrates using NMe4F.

Selective fluorination of pyridine and its derivatives in the presence of high-oxidation-state transition metals

Gryaznova,Khrizanforova,Kholin,Khrizanforov,Budnikova, Yu. H.

, p. 1798 - 1804 (2017/03/22)

The oxidative fluorination of pyridine and 4-ethylpyridine under chemical and electro-chemical conditions in the presence of transition metal (high-oxidation-state nickel, cobalt, and silver) salts was studied. The chemical fluorination affords 2-fluoropyridine in all cases, while the electrochemical fluorination results in 2-fluoroor 3-fluoropyridine depending on the catalyst used.

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