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Benzenepropanoic acid, alpha-fluoro-alpha-methyl-beta-oxo-, methyl ester, (R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144462-33-9

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144462-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144462-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,6 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144462-33:
(8*1)+(7*4)+(6*4)+(5*4)+(4*6)+(3*2)+(2*3)+(1*3)=119
119 % 10 = 9
So 144462-33-9 is a valid CAS Registry Number.

144462-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-methyl 2-fluoro-2-methyl-3-oxo-3-phenyl-propionate

1.2 Other means of identification

Product number -
Other names (R)-2-Fluoro-2-methyl-3-oxo-3-phenyl-propionic acid methyl 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:144462-33-9 SDS

144462-33-9Relevant academic research and scientific papers

Highly enantioselective fluorination reactions of β-ketoesters and β-ketophosphonates catalyzed by chiral palladium complexes

Hamashima, Yoshitaka,Suzuki, Toshiaki,Takano, Hisashi,Shimura, Yuta,Tsuchiya, Yasunori,Moriya, Ken-ichi,Goto, Tomomi,Sodeoka, Mikiko

, p. 7168 - 7179 (2007/10/03)

Using chiral palladium enolates as key intermediates, efficient catalytic enantioselective fluorination reactions of active methine compounds have been developed. These reactions can be conducted in alcoholic solvents without any precaution to exclude wat

Asymmetric fluorination of β-keto esters catalyzed by chiral rare earth perfluorinated organophosphates

Suzuki, Shoko,Furuno, Hiroshi,Yokoyama, Yasuo,Inanaga, Junji

, p. 504 - 507 (2007/10/03)

Novel chiral rare earth metal complexes bearing perfluorinated binaphthyl phosphate ligand RE[(R)-F8BNP]3 (RE = rare earth; F8BNP = 5,5′,6,6′,7,7′,8,8′-octafluoro-1,1′-binaph thyl-2,2′-diyl phosphate) have been synthesized

An efficient enantioselective fluorination of various β-ketoesters catalyzed by chiral palladium complexes

Hamashima, Yoshitaka,Yagi, Kenji,Takano, Hisashi,Tamas, Laszlo,Sodeoka, Mikiko

, p. 14530 - 14531 (2007/10/03)

Reflecting the importance of fluorinated organic compounds in medicinal chemistry, development of an efficient method for catalytic enantioselective fluorination is increasingly desirable. Using a novel palladium complex 2 (1-2.5 mol %), various β-ketoest

A novel enantioselective preparation of α-fluoro-β-keto acids

Iwaoka,Murohashi,Sato,Kaneko

, p. 1025 - 1028 (2007/10/02)

A two-step method for the enantioselective preparation of α-fluorinated β-keto acids from 1,3-dioxin-4-ones having l-menthone as the chiral auxiliary at the 2-position is described. The method consists of fluorination of the dioxinones by molecular fluori

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