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1-Fluoro-10-chlorodecane, with the molecular formula C10H20ClF, is a halogenated alkane that is a fluorinated and chlorinated derivative of decane. This chemical compound is characterized by the presence of both a fluorine and chlorine atom in its structure, which endows it with unique chemical properties. It is commonly utilized in organic synthesis and chemical research as a building block for the creation of more complex molecules.

334-62-3

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334-62-3 Usage

Uses

Used in Organic Synthesis:
1-Fluoro-10-chlorodecane is used as a building block in organic synthesis for the development of more complex molecules. Its unique chemical properties, due to the presence of fluorine and chlorine atoms, make it a valuable component in the synthesis of various organic compounds.
Used in Chemical Research:
In the field of chemical research, 1-Fluoro-10-chlorodecane serves as a valuable compound for studying the effects of halogenation on the properties and reactivity of alkanes. It aids in understanding the behavior of fluorinated and chlorinated derivatives in chemical reactions.
Used in Pharmaceuticals:
1-Fluoro-10-chlorodecane is used as an intermediate in the pharmaceutical industry for the synthesis of various drug molecules. Its unique properties allow for the development of new pharmaceutical compounds with specific therapeutic effects.
Used in Agrochemicals:
In the agrochemical industry, 1-Fluoro-10-chlorodecane is employed as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique chemical properties contribute to the development of effective and targeted agrochemical products.
Used in Material Science:
1-Fluoro-10-chlorodecane is utilized in material science for the development of new materials with specific properties. Its fluorinated and chlorinated nature allows for the creation of materials with tailored characteristics for various applications.
It is important to handle 1-Fluoro-10-chlorodecane with caution due to its potential health and environmental hazards. Proper safety measures should be taken during its use to minimize any risks associated with 1-Fluoro-10-chlorodecane.

Check Digit Verification of cas no

The CAS Registry Mumber 334-62-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 334-62:
(5*3)+(4*3)+(3*4)+(2*6)+(1*2)=53
53 % 10 = 3
So 334-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H20ClF/c11-9-7-5-3-1-2-4-6-8-10-12/h1-10H2

334-62-3SDS

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-10-fluorodecane

1.2 Other means of identification

Product number -
Other names 10-Fluorodecyl chloride

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:334-62-3 SDS

334-62-3Relevant academic research and scientific papers

Deiodinative fluorination of alkyl iodide with p-iodotoluene difluoride

Sawaguchi, Masanori,Hara, Shoji,Nakamura, Yutaka,Ayuba, Shinichi,Fukuhara, Tsuyoshi,Yoneda, Norihiko

, p. 3315 - 3319 (2007/10/03)

Oxidative fluorination of alkyl iodides with p-iodotoluene difluoride (4) was carried out. In the presence of Et3N-4HF, the fluorination reaction of prim-alkyl iodides selectively took place at the iodine position under mild conditions to give the corresponding alkyl fluorides in good yields.

Electrochemical fluorodeiodination of alkyl iodides

Sawaguchi, Masanori,Ayuba, Shinichi,Nakamura, Yutaka,Fukuhara, Tsuyoshi,Hara, Shoji,Yoneda, Norihiko

, p. 999 - 1000 (2007/10/03)

Electrochemical oxidation of alkyl iodides using Et3N-nHF complexes as an electrolyte proceeds under mild conditions to give alkyl fluorides in good yields. The reaction is highly chemoselective and the functional groups in the substrate such as an ester, ketone, chloride, and tosylate could be tolerated under the reaction conditions.

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