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Phosphine oxide, [(1R,2R)-1,2-dimethyl-1,2-ethanediyl]bis[diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192449-15-3

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192449-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192449-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,4,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 192449-15:
(8*1)+(7*9)+(6*2)+(5*4)+(4*4)+(3*9)+(2*1)+(1*5)=153
153 % 10 = 3
So 192449-15-3 is a valid CAS Registry Number.

192449-15-3SDS

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 (R,R)-2,3-Bis(diphenylphosphinoyl)butane

1.2 Other means of identification

Product number -
Other names (2R,3R)-(+)-2,3-bis(diphenylphosphinyl)butane

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:192449-15-3 SDS

192449-15-3Downstream Products

192449-15-3Relevant academic research and scientific papers

METHOD FOR SYNTHESIZING OPTICALLY ACTIVE CARBONYL COMPOUNDS

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Paragraph 0205, (2018/03/25)

The present invention relates to a process for the preparation of an optically active carbonyl compound by asymmetric hydrogenation of a prochiral α,β-unsaturated carbonyl compound with hydrogen in the presence of at least one optically active transition metal catalyst that is soluble in the reaction mixture and which has rhodium as catalytically active transition metal and a chiral, bidentate bisphosphine ligand, wherein the reaction mixture during the hydrogenation of the prochiral α,β-unsaturated carbonyl compound additionally comprises at least one compound of the general formula (I): in which R1, R2: are identical or different and are C6- to C10-aryl which is unsubstituted or carries one or more, e.g. 1, 2, 3, 4 or 5, substituents which are selected from C1- to C6-alkyl, C3- to C6-cycloalkyl, C6- to C10-aryl, C1- to C6-alkoxy and amino;Z is a group CHR3R4 or aryl which is unsubstituted or carries one or more, e.g. 1, 2, 3, 4 or 5, substituents which are selected from C1- to C6-alkyl, C3- to C6-cycloalkyl, C6- to C10-aryl, C1- to C6-alkoxy and amino, wherein R3 and R4 are as defined in the claims and the description.

Process for Preparing Optically Active Diphosphanes

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Page/Page column 9, (2008/12/07)

The present invention relates to a process for preparing optically active bisphosphinylalkanes from the correspondingly substituted, racemic 1,2-diols. The optically active bisphosphinylalkanes which can be obtained in this way are suitable as ligands for preparing chiral transition metal catalysts.

Synthesis of chiraphos via asymmetric hydrogenation of 2,3- bis(diphenylphosphinoyl)-buta-1,3-diene

Beghetto, Valentina,Matteoli, Ugo,Scrivanti, Alberto

, p. 155 - 156 (2007/10/03)

(S,S)-2,3-Bis(diphenylphosphinoyl)butane, an immediate precursor of (S,S)-CHIRAPHOS, can be obtained with 70% de and 71% op via double asymmetric hydrogenation of 2,3-bis(diphenylphosphinoyl)buta-1,3-diene in the presence of Ru-(S)-BINAP catalysts.

Synthesis of the chiral diphosphine ligand 2,3-bis(diphenylphosphino)butane (CHIRAPHOS)

Matteoli, Ugo,Beghetto, Valentina,Schiavon, Cristina,Scrivanti, Alberto,Menchi, Gloria

, p. 1403 - 1409 (2007/10/03)

A new synthesis of CHIRAPHOS starting from readily available 2,3-bis(diphenylphosphinyl)- 1,3-butadiene has been devised. The key step of the synthesis is the hydrogenation of the diene to rac-2,3-bis(diphenylphosphinyl)butane. This reduction can be conve

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