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12-Fluoro-2-dodecanone is a synthetic organic compound characterized by the molecular formula C12H21FO. It is a colorless liquid with a distinct odor and is soluble in organic solvents. This chemical is primarily used in the synthesis of pharmaceuticals and agrochemicals due to its unique fluorinated structure, which can impart specific properties to the final products. The presence of a fluorine atom in the molecule can affect its reactivity, lipophilicity, and metabolic stability, making it a valuable intermediate in the development of new drugs and pesticides. It is important to handle 12-fluoro-2-dodecanone with care due to its potential toxicity and reactivity, and it is typically used in a controlled laboratory setting by professionals who are trained in chemical safety protocols.

593-09-9

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593-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 593-09-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 593-09:
(5*5)+(4*9)+(3*3)+(2*0)+(1*9)=79
79 % 10 = 9
So 593-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H23FO/c1-12(14)10-8-6-4-2-3-5-7-9-11-13/h2-11H2,1H3

593-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 12-fluorododecan-2-one

1.2 Other means of identification

Product number -
Other names 12-Fluor-dodecan-2-on

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:593-09-9 SDS

593-09-9Downstream Products

593-09-9Relevant academic research and scientific papers

A dehydrohalogenation methodology for synthesizing terminal olefins under mild conditions

Berube, Marie,Kamal, Fatima,Roy, Jenny,Poirier, Donald

, p. 3085 - 3091 (2008/02/08)

A new methodology for preparing terminal olefins in good yield by dehydrohalogenation of primary alkyl iodide with tetrabutylammonium fluoride in dimethyl sulfoxide at room temperature is presented. Optimization of the mild reaction conditions and assays on various alkyl iodides are described. Georg Thieme Verlag Stuttgart.

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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