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122795-13-5

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122795-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122795-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,7,9 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122795-13:
(8*1)+(7*2)+(6*2)+(5*7)+(4*9)+(3*5)+(2*1)+(1*3)=125
125 % 10 = 5
So 122795-13-5 is a valid CAS Registry Number.

122795-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-fluoro-2-methyl-3-oxobutanoate

1.2 Other means of identification

Product number -
Other names Ethyl 2-fluoro-2-methylacetoacetate

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:122795-13-5 SDS

122795-13-5Downstream Products

122795-13-5Relevant articles and documents

Elemental fluorine, Part 23: Direct fluorination of β-ketoesters as an approach to enantioselective fluorination

Chambers, Richard D.,Nakano, Takashi,Okazoe, Takashi,Sandford, Graham

, p. 792 - 798 (2009)

Attempts to develop a direct enantioselective fluorination protocol using elemental fluorine and an appropriate Lewis acid and chiral ligand system are described.

Direct fluorination of 1,3-dicarbonyl compounds

Chambers, Richard D.,Greenhall, Martin P.,Hutchinson, John

, p. 1 - 8 (1996)

In acid media, 1,3-diketones and 1,3-keloesters can be fluorinated in high yield and often with high conversion mainly to the corresponding 2-fluoro- compounds. Diesters such as diethyl malonate do not react with fluorine under the same reaction conditions. The mechanism of these reactions has been investigated and while the identity of the electrophilic fluorinating species is uncertain, we believe that the essential features of the reaction pathway are understood. Copyright

Chiral 1H NMR Analysis of Carbonyl Compounds Enabled by Cationic Cobalt Complex

Jang, Sumin,Kim, Hyunwoo

supporting information, (2020/06/04)

We report a newly prepared cationic cobalt(III) complex as a general and efficient chiral solvating agent that discriminates carbonyl compounds including esters, amides, ketones, and aldehydes. This cobalt(III) complex was further utilized to directly analyze both the conversion and the enantiomeric excess at once in the asymmetric fluorination.

Enantioselective fluorination of β-ketoesters using tartrate derived bidentate bioxazoline-Cu(II) complexes

Balaraman, Kaluvu,Vasanthan, Ravichandran,Kesavan, Venkitasamy

, p. 919 - 924 (2013/09/23)

Enantioselective fluorination of aliphatic cyclic and acyclic β-ketoesters was achieved in excellent yield (up to 98%) with moderate to good enantioselectivities (up to 86% ee) using tartrate derived bidentate bioxazoline-Cu(II) complexes. This is the fir

Enantioselective α-fluorination and chlorination of β-ketoesters by cobalt catalyst

Kawatsura, Motoi,Hayashi, Shunsuke,Komatsu, Yuji,Hayase, Shuichi,Itoh, Toshiyuki

experimental part, p. 466 - 467 (2010/08/20)

We demonstrated the cobalt-catalyzed asymmetric a-fluorination and a-chlorination of β-ketoesters. Both reactions were achieved using a catalytic amount of Co(acac)2 with (R, R)Jacobsen's salen ligand; α-fluorinated or a-chlorinated products were thus obt

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