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3-Fluoropropyl benzoate is an organic compound with the chemical formula C10H9FO2. It is a colorless liquid with a molecular weight of 182.17 g/mol. 3-Fluoropropyl=benzoate is characterized by the presence of a benzoate group (a benzene ring with a carboxylate group) and a 3-fluoropropyl chain (a propyl chain with one fluorine atom attached to the third carbon). 3-Fluoropropyl benzoate is synthesized through the esterification of benzoic acid and 3-fluoropropanol, and it is used in various applications, including as a fragrance ingredient and in the production of pharmaceuticals. Its chemical structure and properties make it a valuable intermediate in the synthesis of more complex organic compounds.

614-50-6

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614-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 614-50-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 614-50:
(5*6)+(4*1)+(3*4)+(2*5)+(1*0)=56
56 % 10 = 6
So 614-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11FO2/c11-7-4-8-13-10(12)9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2

614-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-fluoropropyl benzoate

1.2 Other means of identification

Product number -
Other names Benzoesaeure-(3-fluor-propylester)

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:614-50-6 SDS

614-50-6Downstream Products

614-50-6Relevant academic research and scientific papers

Silver-catalyzed radical fluorination of alkylboronates in aqueous solution

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

, 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.

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