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132836-66-9

132836-66-9

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132836-66-9 Usage

Chemical Properties

offwhite crystals

Check Digit Verification of cas no

The CAS Registry Mumber 132836-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132836-66:
(8*1)+(7*3)+(6*2)+(5*8)+(4*3)+(3*6)+(2*6)+(1*6)=129
129 % 10 = 9
So 132836-66-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO3/c1-9(14)13-11(8-16-12(13)15)7-10-5-3-2-4-6-10/h2-6,11H,7-8H2,1H3/t11-/m1/s1

132836-66-9 Well-known Company Product Price

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  • Aldrich

  • (421642)  (S)-(+)-3-Acetyl-4-benzyl-2-oxazolidinone  99%

  • 132836-66-9

  • 421642-5G

  • 1,415.70CNY

  • Detail

132836-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (N-ACETYL)-(4R)-BENZYL-2-OXAZOLIDINONE

1.2 Other means of identification

Product number -
Other names (S)-(+)-3-Acetyl-4-benzyl-2-oxazolidinone

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:132836-66-9 SDS

132836-66-9Relevant articles and documents

Enantioselective multicomponent synthesis of fused 6-5 bicyclic 2-butenolides by a cascade heterobicyclisation process

Suero, Marcos G.,De La Campa, Raquel,Torre-Fernandez, Laura,Garcia-Granda, Santiago,Florez, Josefa

supporting information; experimental part, p. 7287 - 7295 (2012/07/17)

The successive coupling of an alkoxy(aryl/heteroaryl)carbene complex of chromium with either a ketone or an imide lithium enolate and then a 3-substituted (H, TMS, PhCH2, PhCH2CH2, Me) propargylic organomagnesium reagent h

Application of ynamides in the synthesis of 2-amidoindoles

Dooleweerdt, Karin,Ruhland, Thomas,Skrydstrup, Troels

supporting information; experimental part, p. 221 - 224 (2009/06/20)

A Pd-catalyzed, one-pot, two-step synthesis of 2-amidoindoles from ynamides and o-iodoanilines is reported. A key highlight of this sequence is that after the Sonogashira reaction, intramolecular cyclization to the indole occurs spontaneously without acti

Electrogenerated base-induced N-acylation of chiral oxazolidin-2-ones. 2

Feroci, Marta,Inesi, Achille,Palombi, Laura,Sotgiu, Giovanni

, p. 1719 - 1721 (2007/10/03)

An improved and efficient electrochemical N-acylation of chiral oxazolidin-2-ones has been achieved. The generation of the nitrogen anion is obtained under mild conditions and without addition of base or probase, by direct electrolysis of a solution of Me

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