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4-Fluorobutanenitrile, also known as 4-fluoro-1-butanenitrile or 4-fluorobutyl cyanide, is an organic compound with the chemical formula C4H6FN. It is a colorless liquid with a pungent odor and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound consists of a butane chain with a fluorine atom at the fourth carbon position and a nitrile group (CN) at the end. Due to its reactivity and the presence of the fluorine atom, 4-fluorobutanenitrile can undergo various chemical reactions, such as nucleophilic substitution, addition, and elimination, making it a valuable building block in organic synthesis.

407-83-0

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407-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 407-83-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 407-83:
(5*4)+(4*0)+(3*7)+(2*8)+(1*3)=60
60 % 10 = 0
So 407-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H6FN/c5-3-1-2-4-6/h1-3H2

407-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluorobutanenitrile

1.2 Other means of identification

Product number -
Other names BUTYRONITRILE,4-FLUORO

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:407-83-0 SDS

407-83-0Downstream Products

407-83-0Relevant academic research and scientific papers

Photoinduced Remote Functionalisations by Iminyl Radical Promoted C?C and C?H Bond Cleavage Cascades

Dauncey, Elizabeth M.,Morcillo, Sara P.,Douglas, James J.,Sheikh, Nadeem S.,Leonori, Daniele

supporting information, p. 744 - 748 (2017/12/13)

A photoinduced cascade strategy leading to a variety of differentially functionalised nitriles and ketones has been developed. These reactions rely on the oxidative generation of iminyl radicals from simple oximes. Radical transposition by C(sp3)?(sp3) and C(sp3)?H bond cleavage gives access to distal carbon radicals that undergo SH2 functionalisations. These mild, visible-light-mediated procedures can be used for remote fluorination, chlorination, and azidation, and were applied to the modification of bioactive and structurally complex molecules.

Racemic thioesters for production of polyketides

-

, (2008/06/13)

Facile methods for preparing diketide and triketide thioesters are disclosed. The resulting thioesters may be used as intermediates in the synthesis of desired polyketides, and may contain functional groups which ultimately reside in side chains on the resulting polyketide and thus can be used further to manipulate the polyketide so as form derivatives. The polyketides produced may also be tailored by glycosylation, hydroxylation and the like. New polyketides and their derivatives and tailored forms are thereby produced.

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