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2-Butanone, 1-(4-fluorophenyl)-, also known as 1-(4-fluorophenyl)-2-butanone or 4'-fluoracetophenone, is an organic compound with the chemical formula C10H11FO. It is a colorless to pale yellow liquid with a molecular weight of 166.19 g/mol. 2-Butanone, 1-(4-fluorophenyl)- is characterized by the presence of a fluorine atom attached to a phenyl ring, which is connected to a butanone group. It is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is important to handle 2-butanone, 1-(4-fluorophenyl)- with care, following proper safety protocols.

620-97-3

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620-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620-97-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 620-97:
(5*6)+(4*2)+(3*0)+(2*9)+(1*7)=63
63 % 10 = 3
So 620-97-3 is a valid CAS Registry Number.

620-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluorophenyl)butan-2-one

1.2 Other means of identification

Product number -
Other names 1-(4-fluoro-phenyl)-butan-2-one

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:620-97-3 SDS

620-97-3Relevant academic research and scientific papers

Synthesis of 6-substituted 3-(alkoxycarbonyl)-5-aryl-α-pyrones

Miura, Takuya,Fujioka, Saki,Takemura, Naoto,Iwasaki, Hiroki,Ozeki, Minoru,Kojima, Naoto,Yamashita, Masayuki

, p. 496 - 502 (2014/03/21)

An efficient synthesis of 6-substituted 3-(alkoxycarbonyl)-5-aryl-α- pyrones is reported. This methodology consists of the successive manipulation of an addition-elimination reaction between benzyl ketone derivatives and dimethyl methoxymethylenemalonate,

Electroreductive Acylation of Benzyl Chlorides with Acid Anhydrides. Stereoselective Formation of (E)-Enol Esters from Benzyl Alkyl Ketones

Nishiguchi, Ikuzo,Oki, Tsuneo,Hirashima, Tsuneaki,Shiokawa, Jiro

, p. 2005 - 2008 (2007/10/02)

Electroreduction of benzyl chlorides in the presence of acid anhydrides brought about stereoselective formation of (E)-enol esters of the corresponding benzyl alkyl ketones, the initial acylated products, in good to moderate yields.

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