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201300-96-1

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201300-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201300-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,3,0 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 201300-96:
(8*2)+(7*0)+(6*1)+(5*3)+(4*0)+(3*0)+(2*9)+(1*6)=61
61 % 10 = 1
So 201300-96-1 is a valid CAS Registry Number.

201300-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-bromopropionyl)-4R-phenyloxazolidin-2-one

1.2 Other means of identification

Product number -
Other names 3-(2-bromopropionyl)-4R-phenyl-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:201300-96-1 SDS

201300-96-1Relevant articles and documents

Stereoselective dimerization of chiral α-bromoamides promoted by Fe(Co)5

Kuznetsov,Khrustalev,Terentiev,Belokon'

, p. 548 - 550 (2007/10/03)

Organic α-bromocarboxylates react with aldehydes and ketones in the presence of Fe(CO)5 (the Reformatsky-type reactions). Unlike them, N-oxazolidinone derivatives of the same acids undergo diastereoselective reductive dimerization to give (2S,3S)-dimers, regardless of the configuration of the α-chiral center in the starting reagent.

Heterocyclic compounds and their production

-

, (2008/06/13)

A compound of the formula: STR1 wherein R1, R2, R3 and R4 are each a hydrogen atom, a lower alkyl group, an ar(lower)alkyl group or an aryl group, or R1 and R2 may be combined together to f

A highly stereoselective synthesis of a key intermediate of 1β-methylcarbapenems employing the Reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives

Ito,Terashima

, p. 6625 - 6628,6625-6628 (2007/10/02)

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