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1-Chloro-4-fluorobutane, with the chemical formula C4H8ClF, is a synthetic halogenated compound that exists as a colorless liquid at room temperature. It is characterized by the presence of both a chlorine and a fluorine atom, which endows it with high chemical reactivity, making it a versatile reagent in various applications.

462-73-7

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462-73-7 Usage

Uses

Used in Chemical Research:
1-Chloro-4-fluorobutane is used as a reagent in chemical research for its unique properties and reactivity, facilitating the synthesis of various organic compounds.
Used in Pharmaceutical Production:
1-Chloro-4-fluorobutane is used as an intermediate in the production of pharmaceuticals, contributing to the development of new drugs and medicines.
Used in the Synthesis of Organic Compounds:
Due to its chemical reactivity, 1-Chloro-4-fluorobutane is used as a building block in the synthesis of a wide range of organic compounds, including specialty chemicals and materials.
Safety and Storage:
1-Chloro-4-fluorobutane should be stored in a cool, dry, and well-ventilated place, away from heat sources and open flames to prevent potential hazards. It is essential to handle this chemical substance under controlled conditions and with appropriate personal protective equipment to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 462-73-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 462-73:
(5*4)+(4*6)+(3*2)+(2*7)+(1*3)=67
67 % 10 = 7
So 462-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H8ClF/c5-3-1-2-4-6/h1-4H2

462-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-fluorobutane

1.2 Other means of identification

Product number -
Other names 1-chloro-4-fluoro-butane

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:462-73-7 SDS

462-73-7Relevant academic research and scientific papers

REACTIONS OF HALOGEN FLUORIDES. XI. MECHANISM OF REACTIONS OF ALKYL HALIDES WITH BROMINE TRIFLUORIDE

Kartashov, A. V.,Chuvatkin, N. N.,Kurskii, Yu. A.,Boguslavskaya, L. S.

, p. 2279 - 2284 (2007/10/02)

The effects of the substituted halogen, the neighboring groups, and the polarity of the medium on the nature of the fluorination products were studied for the reactions of δ-substituted halogenobutanes and 1,2,3-trihalogenobutanes with bromine tetrachloride.A mechanism involving formation of linear halogenonium ions at the rate-determining stage is proposed.

FLUORINATION OF HALOGENO ALCOHOLS WITH 1,1,2,3,3,3-HEXAFLUOROPROPYL DIETHYLAMINE

Watanabe, S.,Fujita, T.,Usui, Y.,Kimura, Y.

, p. 135 - 142 (2007/10/02)

Fluorination of halogeno alcohols with 1,1,2,3,3,3-hexafluoropropyl diethylamine (PPDA) was investigated. 2-Bromo-1-fluorobutane was obtained from the reaction of PPDA and 2-bromo-1-butanol (yield 50percent).Similar results were obtained from other alipha

Free Radical Substitution. Part 37. The Effect of Solvent on the Atomic Chlorination of 1-Substituted Butanes and Related Compounds

Potter, Alan,Tedder, John M.

, p. 1689 - 1692 (2007/10/02)

Experimental results reported in this paper show that the relative selectivity of atomic chlorination of 1-substituted butanes and related compounds is greatly influenced by the phase and by solvents.Solvents can be divided into three classes: (a) inert, (b) solvents which decrease the selectivity, and (c) solvents which increase the selectivity.The second group solvate the transition state and the third group solvate the chlorine atoms.

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