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139139-93-8

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  • [(1S)-5,5',6,6',7,7',8,8'-Octahydro-(1,1'-binaphthalene)-2,2'-diyl]-bis-(diphenylphosphine)

    Cas No: 139139-93-8

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139139-93-8 Usage

Reactions

Biaryl bisphosphine ligand. The H8-BINAP ligand, as the ruthenium complex, catalyzes hydrogenation of unsaturated carboxylic acids to a higher ee than does BINAP. The ruthenium catalyzed hydrogenation of aryl propenoic acid to produce the drug Ibuprofen. Rhodium catalyzed asymmetric regioselective 1,4-addition of arylboronic acids to 3-substituted maleimides. Ligand for palladium-catalyzed enantioselective hydrogenation of substituted indoles. Rhodium-catalyzed enantioselective cyclization of γ-alkynylaldehydes with acyl phosphonates. Enantioselective synthesis of axially chiral 1-arylisoquinolines by Rh-catalyzed [2+2+2] cycloaddition. Enantioselective synthesis of 2,3-disubstituted indolines through Bronsted acid/Pd-complex-promoted tandem reactions.

Uses

Takasago Ligands and Complexes for Asymmetric Reactions

Check Digit Verification of cas no

The CAS Registry Mumber 139139-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,3 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139139-93:
(8*1)+(7*3)+(6*9)+(5*1)+(4*3)+(3*9)+(2*9)+(1*3)=148
148 % 10 = 8
So 139139-93-8 is a valid CAS Registry Number.

139139-93-8 Well-known Company Product Price

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  • Aldrich

  • (693014)  (S)-H8-BINAP  technical grade

  • 139139-93-8

  • 693014-50MG

  • 819.00CNY

  • Detail
  • Aldrich

  • (693014)  (S)-H8-BINAP  technical grade

  • 139139-93-8

  • 693014-100MG

  • 1,547.91CNY

  • Detail

139139-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5',6,6',7,7',8,8'-Octahydro-1,1'-binaphthalene-2,2'-diylbis(dip henylphosphine)

1.2 Other means of identification

Product number -
Other names 2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl

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:139139-93-8 SDS

139139-93-8Downstream Products

139139-93-8Relevant articles and documents

NOVEL RUTHENIUM COMPLEX AND PROCESS FOR PRODUCING OPTICALLY ACTIVE ALCOHOL COMPOUND USING SAME AS CATALYST

-

Paragraph 0064, (2014/03/21)

The present invention provides: a novel ruthenium complex which has excellent catalytic activity with respect to reactivity in the reduction of a multiple bond, in particular, in the asymmetric reduction of a carbonyl compound, enantioselectivity, etc.; a catalyst which comprises the ruthenium complex; and a process for producing optically active compound, in particular, an optically active alcohol compound, using the catalyst. The ruthenium complex has a ruthenacyclic structure. The catalyst is a catalyst for asymmetric reduction which comprises the ruthenium complex.

Method for making an optically active diphosphine ligand

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, (2008/06/13)

The present invention provides a method for making compound (1) by reacting compound (2) with phosphine oxide (3) in the presence of a transition metal/phosphine complex and optionally reducing the reaction product: STR1 where n represents 0 or 1; the double line having a continuous line and a dotted line represents a double bond or a single bond such that the ring having the double line forms a naphthalene ring or an octahydronaphthalene ring with an adjacent benzene ring; Tf represents a trifluoromethanesulfonyl group; and Ar represents a phenyl group, a substituted phenyl group or a naphthyl group. The present invention provides an economical way to produce compound (1) as a ligand of a complex useful as a catalyst for a variety of asymmetric synthesis reactions.

Synthesis of Partially Hydrogenated BINAP Variants

Zhang, Xiaoyong,Mashima, Kazushi,Koyano, Kinko,Sayo, Noboru,Kumobayashi, Hidenori,et al.

, p. 7283 - 7286 (2007/10/02)

Three pairs of new axially dissymmetric diphosphine ligands, (R)-(-)- and (S)-(+)-2,2'-bis(dicyclohexylphosphino)-1,1'-binaphthyl , (R)-(+)- and (S)-(-)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphth

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