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Ethyl 6-fluorohexanoate is an organic compound with the chemical formula C8H15FO2. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 166.20 g/mol. This ester is derived from the combination of 6-fluorohexanoic acid and ethanol, featuring a fluorine atom in the sixth carbon position of the hexanoate chain. Ethyl 6-fluorohexanoate is primarily used as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals, owing to its unique properties and reactivity. It is also known for its potential applications in the development of new materials with enhanced properties, such as improved thermal stability and reduced flammability.

589-79-7

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589-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 589-79-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 589-79:
(5*5)+(4*8)+(3*9)+(2*7)+(1*9)=107
107 % 10 = 7
So 589-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H15FO2/c1-2-11-8(10)6-4-3-5-7-9/h2-7H2,1H3

589-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-fluorohexanoate

1.2 Other means of identification

Product number -
Other names 6-fluoro-hexanoic 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:589-79-7 SDS

589-79-7Downstream Products

589-79-7Relevant academic research and scientific papers

XANOMELINE DERIVATIVES AND METHODS FOR TREATING NEUROLOGICAL DISORDERS

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Paragraph 0212, (2021/05/21)

Provided herein are compounds comprising compounds of formula (I) and/or salts thereof; wherein at least one of R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, and R13 is fluorine, and the remainder are independently chosen from hydrogen and fluorine; and R14, R15, R16, R17, R18, R19, R20, R21, R22, and R23 are independently chosen from hydrogen and deuterium; with the proviso that when R1, R2, and R3 are fluorine, then at least one of R4, R5, R6, R7, R8, R9, R10, R11, R12, and R13 is fluorine or at least one of R14, R15, R16, R17, R18, R19, R20, R21, R22, and R23is deuterium. Also provided are medicaments comprising these compounds and methods for treating central nervous system disorders with the compounds and medicaments described herein.

Efficient SN2 fluorination of primary and secondary alkyl bromides by copper(I) fluoride complexes

Liu, Yanpin,Chen, Chaohuang,Li, Huaifeng,Huang, Kuo-Wei,Tan, Jianwei,Weng, Zhiqiang

, p. 6587 - 6592 (2013/12/04)

Copper(I) fluoride complexes ligated by phenanthroline derivatives have been synthesized and structurally characterized by X-ray crystallography. These complexes adopt as either ionic or neutral forms in the solid state, depending on the steric bulkiness of the substituent groups on the phenanthroline ligands. These complexes react with primary and secondary alkyl bromides to produce the corresponding alkyl fluorides in modest to good yields. This new method is compatible with a variety of important functional groups such as ether, thioether, amide, nitrile, methoxyl, hydroxyl, ketone, ester, and heterocycle moieties.

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