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87214-07-1

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87214-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87214-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87214-07:
(7*8)+(6*7)+(5*2)+(4*1)+(3*4)+(2*0)+(1*7)=131
131 % 10 = 1
So 87214-07-1 is a valid CAS Registry Number.

87214-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4S,5R)-2,3,4,5-tetrahydro-3,4-dimethyl-2,5-diphenyl-1,3,2-oxazaphosphole

1.2 Other means of identification

Product number -
Other names (2R,4S,5R)-3,4,Dimethyl-2,5-diphenyl-1,3,2-oxazaphospholidin

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:87214-07-1 SDS

87214-07-1Relevant articles and documents

Synthesis of P-chirogenic diarylphosphinoacetic acids and their proline derivatives for palladium-catalysed allylic alkylation reactions

Lam, Hubert,Horton, Peter N.,Hursthouse, Michael B.,Aldous, David J.,King, Kuok Hii

, p. 8145 - 8148 (2007/10/03)

The synthesis of P-chirogenic diarylphosphinocarboxylic acids was achieved, from which a new class of amido- and amino-diphosphine ligands (PNP*) were derived, containing an L-proline backbone. The catalytic activities of the novel ligands were evaluated

A flexible, highly efficient method for the preparation of homochiral oxazaphospholidine-boranes

Sheehan, Susan Kult,Jiang, Meiqun,McKinstry, Lydia,Livinghouse, Tom,Garton, Donna

, p. 6155 - 6162 (2007/10/02)

An efficient and operationally simple procedure for the synthesis of 2-substituted 3,4-dimethyl-5-phenyloxazaphospholidine derivatives has been developed. This new method permits the large scale preparation of a range of electronically and sterically diff

Asymmetric synthesis of phosphinates, phosphine oxides and phosphines by Michaelis Arbuzov rearrangement of chiral oxazaphospholidine

Juge, S.,Genet, J. P.

, p. 2783 - 2786 (2007/10/02)

A general approach to asymmetric synthesis of high optically active tertiary organophosphorus compounds is described.Oxazaphospholidine 3 reacts with alkyl halide to give regio and stereoselectively the corresponding phosphinamide 4.Methyl phenyl phosphin

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