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Chloro(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl [(2R)-(-)-1-(4-Methoxyphenyl)1 (4-Methoxyphenyl-kC)-3Methyl-1,2-butanediaMine]rutheniuM(II) (R)-RUCY XylBINAP is a complex chemical compound that features ruthenium(II) coordinated with a chiral bisphosphine ligand and a chiral amine ligand. Chloro(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl [(2R)-(-)-1-(4-Methoxyphenyl)1 (4-Methoxyphenyl-kC)-3Methyl-1,2-butanediaMine]rutheniuM(II) (R)-RUCY XylBINAP's chiral nature, due to the specific arrangement of its ligands, allows for the existence of different stereoisomeric forms. The presence of a chlorine ligand and the unique chemical properties of the compound make it a promising candidate for applications in asymmetric catalysis and other chemical reactions.

1384974-38-2

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1384974-38-2 Usage

Uses

Used in Asymmetric Catalysis:
Chloro(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl [(2R)-(-)-1-(4-Methoxyphenyl)1 (4-Methoxyphenyl-kC)-3Methyl-1,2-butanediaMine]rutheniuM(II) (R)-RUCY XylBINAP is used as a catalyst in asymmetric catalysis for its ability to selectively produce enantiomerically pure products. The chiral bisphosphine and amine ligands contribute to the compound's effectiveness in creating chiral centers in target molecules, which is crucial in the synthesis of pharmaceuticals and agrochemicals.
Used in Chemical Reactions:
In the chemical industry, Chloro(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl [(2R)-(-)-1-(4-Methoxyphenyl)1 (4-Methoxyphenyl-kC)-3Methyl-1,2-butanediaMine]rutheniuM(II) (R)-RUCY XylBINAP is used as a catalyst or reagent in various chemical reactions. Its unique properties allow it to facilitate transformations that may not be possible with other catalysts or reagents, leading to the production of desired products with high yields and selectivity.
Used in Research and Development:
Chloro(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl [(2R)-(-)-1-(4-Methoxyphenyl)1 (4-Methoxyphenyl-kC)-3Methyl-1,2-butanediaMine]rutheniuM(II) (R)-RUCY XylBINAP is utilized in research and development settings to explore new chemical reactions, investigate the compound's catalytic properties, and develop new methodologies for synthesizing complex molecules. Its unique structure and potential applications make it an interesting subject for academic and industrial research.

Check Digit Verification of cas no

The CAS Registry Mumber 1384974-38-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,9,7 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1384974-38:
(9*1)+(8*3)+(7*8)+(6*4)+(5*9)+(4*7)+(3*4)+(2*3)+(1*8)=212
212 % 10 = 2
So 1384974-38-2 is a valid CAS Registry Number.

1384974-38-2 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (R0139)  (R)-RUCY®-XylBINAP  

  • 1384974-38-2

  • 200mg

  • 520.00CNY

  • Detail
  • TCI America

  • (R0139)  (R)-RUCY®-XylBINAP  

  • 1384974-38-2

  • 1g

  • 1,880.00CNY

  • Detail

1384974-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-RUCY?-XylBINAP

1.2 Other means of identification

Product number -
Other names RuCl[()-daipena][()-xylbinap]

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:1384974-38-2 SDS

1384974-38-2Downstream Products

1384974-38-2Relevant academic research and scientific papers

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

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Paragraph 0099, (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.

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