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6-Fluorohexanenitrile is an organic compound with the chemical formula C6H10FN. It is a colorless liquid with a molecular weight of 115.15 g/mol. 6-fluorohexanenitrile is characterized by the presence of a fluorine atom at the 6th carbon position in a hexane chain, with a nitrile group (CN) attached to the terminal carbon. 6-Fluorohexanenitrile is synthesized through various chemical reactions and is used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential toxicity, it is important to handle 6-fluorohexanenitrile with care and in accordance with safety guidelines.

373-31-9

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373-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 373-31-9 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 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 373-31:
(5*3)+(4*7)+(3*3)+(2*3)+(1*1)=59
59 % 10 = 9
So 373-31-9 is a valid CAS Registry Number.

373-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Fluorohexanonitrile

1.2 Other means of identification

Product number -
Other names -

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

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More Details:373-31-9 SDS

373-31-9Relevant academic research and scientific papers

Silver-catalyzed radical fluorination of alkylboronates in aqueous solution

Li, Zhaodong,Wang, Zhentao,Zhu, Lin,Tan, Xinqiang,Li, Chaozhong

supporting information, p. 16439 - 16443 (2015/01/09)

We report herein an efficient and general method for the deboronofluorination of alkylboronates. Thus, with the catalysis of AgNO3, the reactions of various alkylboronic acids or their pinacol esters with Selectfluor reagent in acidic aqueous solution afforded the corresponding alkyl fluorides under mild conditions. A broad substrate scope and wide functional group compatibility were observed. A radical mechanism is proposed for this site-specific fluorination.

Approaches towards the synthesis of fluoro(cyclo)alkylamines

Windhorst,Bechger,Visser,Menge,Leurs,Timmerman,Herscheid

, p. 35 - 40 (2007/10/03)

The synthesis of fluoro(cyclo)alkylamines 1-amino-6-fluorohexane (1), 1-amino-7-fluoroheptane (2), cis/trans-4-fluorocyclohexylamine (3a,b) and cis-4-fluoromethylcyclohexylamine (4) has been investigated for use as synthons for histamine receptor ligands for use in PET.

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