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Octanoic acid, 2-fluoro, ethyl ester, also known as 2-fluorooctanoic acid ethyl ester, is an organic compound with the chemical formula C10H19FO2. It is a colorless liquid at room temperature and is derived from the esterification of 2-fluorooctanoic acid and ethanol. Octanoic acid, 2-fluoro-, ethyl ester is characterized by its unique fluorinated chain, which imparts distinct chemical and physical properties compared to its non-fluorinated counterparts. It is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals, where the presence of fluorine can significantly alter the reactivity, lipophilicity, and metabolic stability of the final product. The ester group in the molecule also plays a crucial role in determining its reactivity and potential uses in chemical reactions.

7740-65-0

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7740-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7740-65-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,4 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7740-65:
(6*7)+(5*7)+(4*4)+(3*0)+(2*6)+(1*5)=110
110 % 10 = 0
So 7740-65-0 is a valid CAS Registry Number.

7740-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-fluorooctanoate

1.2 Other means of identification

Product number -
Other names 2-fluoro-octanoic acid ethyl ester

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:7740-65-0 SDS

7740-65-0Downstream Products

7740-65-0Relevant academic research and scientific papers

Nickel Catalyzed Reaction of Iodofluoroacetates with Alkenes as a Facile Route to α-Fluoroesters

Wang, Yong,Yang, Zhen-Yu,Burton, Donald J.

, p. 2137 - 2140 (2007/10/02)

Reaction of iodofluoroacetates with alkenes and zinc in the presence of nickel dichloride hexahydrate and pyridine in THF affords the corresponding α-fluoroesters in good yields.

Studies on Organic Fluorine Compounds. Part 37. Studies on Steroids. Part 78. Synthesis of 24,24-Difluoro- and 24ξ-Fluoro-25-hydroxyvitamin D3

Kobayashi, Yoshiro,Taguchi, Takeo,Terada, Tadafumi,Oshida, Jun-ichi,Morisaki, Masuo,Ikekawa, Nobuo

, p. 85 - 92 (2007/10/02)

To clarify the physiological significance of C-24 hydroxylation in vitamin D3 metabolism , vitamin D3 compounds blocked at C-24 by fluorine substituents, namely 24,24-difluoro-25-hydroxyvitamin D3 (1) and 24ξ-fluoro-25-hydroxyvitamin D3 (2) have been synthesized from 3β-hydroxychol-5-en-24-oic acid (13).

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