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Benzenebutanoic acid, 2-fluoro-a-methyl-b-oxo-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

221121-41-1

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221121-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221121-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,2 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 221121-41:
(8*2)+(7*2)+(6*1)+(5*1)+(4*2)+(3*1)+(2*4)+(1*1)=61
61 % 10 = 1
So 221121-41-1 is a valid CAS Registry Number.

221121-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(2-fluorophenyl)-2-methyl-3-oxobutyrate

1.2 Other means of identification

Product number -
Other names 4-(2-Fluoro-phenyl)-2-methyl-3-oxo-butyric 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:221121-41-1 SDS

221121-41-1Relevant academic research and scientific papers

Synthesis of Novel Chiral Benzophospholanes and Their Application in Asymmetric Hydrogenation

Shimizu, Hideo,Saito, Takao,Kumobayashi, Hidenori

, p. 185 - 189 (2007/10/03)

A new class of chiral ligands bearing one or two benzophospholanes was developed for the purpose of Ru-catalyzed asymmetric hydrogenation. Although results of the Ru catalysis remain insufficient so far, 1,2-bis(2-isopropyl-2,3- dihydro-1H-phosphindol-1-yl)benzene (iPr-BeePHOS: 2b) has been found to provide high enantioselectivity in the Rh-catalyzed asymmetric hydrogenation of an enamide.

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