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5-Oxazolidinone, 3-benzoyl-2-(1,1-dimethylethyl)-4-methylene-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113304-18-0

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113304-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113304-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,0 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113304-18:
(8*1)+(7*1)+(6*3)+(5*3)+(4*0)+(3*4)+(2*1)+(1*8)=70
70 % 10 = 0
So 113304-18-0 is a valid CAS Registry Number.

113304-18-0SDS

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 N-benzoyl-2(S)-tert-butyl-4-methylene-1,3-oxazolidin-5-one

1.2 Other means of identification

Product number -
Other names (S)-3-Benzoyl-2-tert-butyl-4-methylene-oxazolidin-5-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:113304-18-0 SDS

113304-18-0Relevant academic research and scientific papers

Asymmetric Synthesis of Chiral Cyclic Amino Acids by Diels-Alder Reactions of (2S)- and (2R)-4-Methyleneoxazolidin-5-ones

Pyne, Stephen G.,Dikic, Branko,Gordon, Peter A.,Skelton, Brian W.,White, Allan H.

, p. 73 - 93 (2007/10/02)

The synthesis of chiral (2S)- and (2R)-4-methyleneoxazolidin-5-ones, in high enantiomeric purity from (S)-S-methylcysteine, and their highly exo-selective Diels-Alder reactions with cyclic dienes are described. (1R,2S,4S)-2-Aminobicycloheptane-2-ca

An Efficient Synthesis of (2S)- and (2R)-N-Benzoyl-2-t-butyl-4-methyleneoxazolidin-5-one

Beckwith, Athelstan L. J.,Pyne, Stephen G.,Dikic, Branko,Chai, Christina L. L.,Gordon, Peter A.,et al.

, p. 1425 - 1430 (2007/10/02)

An efficient synthesis of the title compounds in high enantiomeric purity (>98percent) involves bromination under photolytic conditions of (2S)- or (2R)-oxazolidinones derived from (S)-alanine followed by treatment of the products with sodium iodide in re

Diastereoselective Radical Addition to Derivatives of Dehydroalanine and of Dehydrolactic Acid

Beckwith, Athelstan L. J.,Chai, Christina L. L.

, p. 1087 - 1088 (2007/10/02)

The cyclic methylene compounds (1)-(3) undergo diastereoselective free radical addition when treated with alkylmercury hydride or alkyl iodide/tributylstannane to give products useful for the enantioselective synthesis of α-amino and α-hydroxy acids.

104. Bromination of Cyclic Acetals from α-Amino Acids and α- or β-Hydroxy Acids with N-Bromosuccinimide

Zimmermann, Juerg,Seebach, Dieter

, p. 1104 - 1114 (2007/10/02)

The preparation of novel electrophylic building blocks for the synthesis of enantiomerically pure compounds (EPC) is described.Thus, the 2-(tert-butyl)dioxolanones, -oxazolidinones, -imidazolidinones, and -dioxanones obtained by acetalization of pivalalde

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