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394-47-8

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394-47-8 Usage

Description

2-Fluorobenzonitrile, also known as o-fluorobenzonitrile, is an organic aromatic fluoride that is a colorless to light yellow liquid. It is characterized by its reactivity with lithium N,N-dialkylaminoborohydride reagent, which results in the formation of 2-(N,N-dialkylamino)benzylamines.

Uses

Used in Pharmaceutical Industry:
2-Fluorobenzonitrile is used as an intermediate for the synthesis of various pharmaceutical compounds, including 3-amino-1,2-benzisoxazoles, 6-(acetylaminomethyl)-3-amino-1,2-benzisoxazole, and 5-(4′-methyl [1,1′-biphenyl]-2-yl)-1H-tetrazole. Its application in this industry is due to its ability to serve as a building block for the development of new drugs.
Used in Pesticide Industry:
2-Fluorobenzonitrile is used as a chemical intermediate in the production of certain pesticides. The introduction of the fluorine atom into the molecule enhances the properties of the final product, making it more effective and environmentally friendly.
Used in Dye Industry:
2-Fluorobenzonitrile is used as a chemical intermediate in the dyestuff industry. The presence of the fluorine atom in the molecule results in dyed products that are bright, colorful, and less likely to fade, providing a competitive advantage over non-fluorinated alternatives.

Synthesis

Tetramethylammonium fluoride (TMAF) has been found to be an effective fluorodenitration reagent. The good selectivity for the fluoroaromatic and not the phenol has been attributed to the stability of ion pairing between nitrite and tetramethylammonium ions. TMAF reacts with 2-nitrobenzonitrile to give a quantitative conversion to 2-fluorobenzonitrile.

Check Digit Verification of cas no

The CAS Registry Mumber 394-47-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 394-47:
(5*3)+(4*9)+(3*4)+(2*4)+(1*7)=78
78 % 10 = 8
So 394-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H4FN/c8-7-4-2-1-3-6(7)5-9/h1-4H

394-47-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A14375)  2-Fluorobenzonitrile, 99%   

  • 394-47-8

  • 10g

  • 457.0CNY

  • Detail
  • Alfa Aesar

  • (A14375)  2-Fluorobenzonitrile, 99%   

  • 394-47-8

  • 50g

  • 789.0CNY

  • Detail
  • Alfa Aesar

  • (A14375)  2-Fluorobenzonitrile, 99%   

  • 394-47-8

  • 100g

  • 1414.0CNY

  • Detail
  • Alfa Aesar

  • (A14375)  2-Fluorobenzonitrile, 99%   

  • 394-47-8

  • 250g

  • 3029.0CNY

  • Detail

394-47-8SDS

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-Fluorobenzonitrile

1.2 Other means of identification

Product number -
Other names 2-Fluorobenzenenitrile

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:394-47-8 SDS

394-47-8Relevant articles and documents

Visible Light Generation of a Microsecond Long-Lived Potent Reducing Agent

Hu, Ke,Li, Pengju,Meyer, Gerald J.,Niu, Fushuang,Wang, Hanqi,Zhang, Zhenghao,Zhao, Zijian

supporting information, (2022/03/27)

Photoexcitation of molecular radicals can produce strong reducing agents; however, the limited lifetimes of the doublet excited states preclude many applications. Herein, we propose and demonstrate a general strategy to translate a highly energetic electron from a doublet excited state to a ZrO2insulator, thereby increasing the lifetime by about 6 orders of magnitude while maintaining a reducing potential less than -2.4 V vs SCE. Specifically, red light excitation of a salicylic acid modified perylene diimide radical anion PDI?-anchored to a ZrO2insulator yields a ZrO2(e-)|PDI charge separated state with an ~10 μs lifetime in 23% yield. The ZrO2(e-)s were shown to drive CO2→ CO reduction with a Re catalyst present in micromolar concentrations. More broadly, this strategy provides new opportunities to reduce important reagents and catalysts at low concentrations through diffusional electron transfer.

Method for efficiently synthesizing fluorine-containing compound

-

Paragraph 0036-0054, (2021/06/26)

The invention discloses a method for efficiently synthesizing a fluorine-containing compound, and relates to the field of fluorine-containing compound synthesis. The method is a method for generating a corresponding fluorine atom substituted fluorine-containing compound by reacting aromatic chloride or activated chloride serving as a raw material with potassium fluoride under the action of a novel catalyst. The method disclosed by the invention has the advantages of good product selectivity, high efficiency, mild reaction conditions, simplicity and convenience in operation, convenience in application and the like.

Nickel-Catalyzed Reversible Functional Group Metathesis between Aryl Nitriles and Aryl Thioethers

Delcaillau, Tristan,Boehm, Philip,Morandi, Bill

, p. 3723 - 3728 (2021/04/07)

We describe a new functional group metathesis between aryl nitriles and aryl thioethers. The catalytic system nickel/dcype is essential to achieve this fully reversible transformation in good to excellent yields. Furthermore, the cyanide- and thiol-free reaction shows high functional group tolerance and great efficiency for the late-stage derivatization of commercial molecules. Finally, synthetic applications demonstrate its versatility and utility in multistep synthesis.

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