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2-Oxazolidinone, 5,5-dimethyl-3-(1-oxopropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

223906-48-7

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223906-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223906-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,9,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 223906-48:
(8*2)+(7*2)+(6*3)+(5*9)+(4*0)+(3*6)+(2*4)+(1*8)=127
127 % 10 = 7
So 223906-48-7 is a valid CAS Registry Number.

223906-48-7SDS

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 N-Propionyl-5,5-dimethyloxazolidin-2-one

1.2 Other means of identification

Product number -
Other names 5,5-Dimethyl-3-propionyl-oxazolidin-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:223906-48-7 SDS

223906-48-7Relevant academic research and scientific papers

Valence tautomerism in titanium enolates: Catalytic radical haloalkylation and application in the total synthesis of neodysidenin

Beaumont, Stephane,Ilardi, Elizabeth A.,Monroe, Lucas R.,Zakarian, Armen

supporting information; experimental part, p. 1482 - 1483 (2010/04/03)

(Chemical Equation Presented) A direct ruthenium-catalyzed radical chloroalkylation of N-acyl oxazolidinones capitalizing on valence tautomerism of titanium enolates has been developed. The chloroalkylation method served as the centerpiece in the enantioselective total synthesis of trichloroleucine-derived marine natural product neodysidenin.

Asymmetric alkylations using SuperQuat auxiliaries - An investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones

Bull, Steven D.,Davies, Stephen G.,Jones, Simon,Sanganee, Hitesh J.

, p. 387 - 398 (2007/10/03)

Studies on the alkylation of enolates derived from a range of N-acyl-5,5-dimethyloxazolidin-2-ones and N-acyl-5,5-diphenyloxazolidin-2-ones reveal that high yields and high diastereoselectivities are best obtained when homochiral 4-isopropyl-5,5-dimethyloxazolidin-2-one is employed as a chiral auxiliary.

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