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851530-57-9

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851530-57-9 Usage

Description

Bis(2,2-dimethylpropanoato)(4-methylphenyl)bis[tris[4-(trifluoromethyl)phenyl]phosphine]rhodium is a complex chemical compound that contains rhodium as its central metal atom. Bis(2,2-dimethylpropanoato)(4-methylphenyl)bis[tris[4-(trifluoromethyl)phenyl]phosphine]rhodium also includes two ligands of 2,2-dimethylpropanoato and a 4-methylphenyl, as well as a bis(tris[4-(trifluoromethyl)phenyl]phosphine) group. It is known for its unique reactivity and stability, which makes it a promising candidate for use in various organic synthesis reactions.

Uses

Used in Organic Synthesis:
Bis(2,2-dimethylpropanoato)(4-methylphenyl)bis[tris[4-(trifluoromethyl)phenyl]phosphine]rhodium is used as a catalyst for various organic synthesis reactions. Its unique structure and properties allow it to facilitate a wide range of reactions in the field of organic chemistry, making it a valuable tool for chemists.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Bis(2,2-dimethylpropanoato)(4-methylphenyl)bis[tris[4-(trifluoromethyl)phenyl]phosphine]rhodium is used as a catalyst for the synthesis of complex organic molecules, including those used in the development of new drugs. Its ability to catalyze a variety of reactions makes it a versatile and essential component in the synthesis of pharmaceutical compounds.
Used in Chemical Research:
Bis(2,2-dimethylpropanoato)(4-methylphenyl)bis[tris[4-(trifluoromethyl)phenyl]phosphine]rhodium is also used in chemical research as a catalyst for studying reaction mechanisms and exploring new synthetic pathways. Its unique reactivity and stability make it an ideal candidate for investigating novel reactions and understanding the underlying chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 851530-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,5,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 851530-57:
(8*8)+(7*5)+(6*1)+(5*5)+(4*3)+(3*0)+(2*5)+(1*7)=159
159 % 10 = 9
So 851530-57-9 is a valid CAS Registry Number.

851530-57-9 Well-known Company Product Price

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  • Aldrich

  • (695181)  Bis(2,2-dimethylpropanoato)(4-methylphenyl)bis[tris[4-(trifluoromethyl)phenyl]phosphine]rhodium  

  • 851530-57-9

  • 695181-100MG

  • 1,199.25CNY

  • Detail
  • Aldrich

  • (695181)  Bis(2,2-dimethylpropanoato)(4-methylphenyl)bis[tris[4-(trifluoromethyl)phenyl]phosphine]rhodium  

  • 851530-57-9

  • 695181-500MG

  • 3,967.47CNY

  • Detail

851530-57-9SDS

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 2,2-dimethylpropanoic acid,methylbenzene,rhodium,tris[4-(trifluoromethyl)phenyl]phosphane

1.2 Other means of identification

Product number -
Other names [(p-CF3-C6H4)3P]2 bis(pivalate) rhodium(I)(p-tolyl)

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:851530-57-9 SDS

851530-57-9Downstream Products

851530-57-9Relevant articles and documents

Direct C-arylation of free (NH)-indoles and pyrroles catalyzed by Ar-Rh(III) complexes assembled in situ

Wang, Xiang,Lane, Benjamin S.,Sames, Dalibor

, p. 4996 - 4997 (2007/10/03)

Ar-Rh(III) pivalate complexes assembled in situ from the reaction of [RhCl(coe)2]2 (coe = cis-cyclooctene), [p-(CF3)C6H4]3P, and CsOPiv effectively catalyzed the direct C-arylation of free (NH)-indoles and (NH)-pyrroles in good yields and with high regioselectivity. The reaction displayed excellent functional group compatibility and low moisture sensitivity. Kinetics studies support a mechanism involving phosphine displacement by indole in complex 2 (resting state of the catalyst), followed by a rate-limiting C-H bond metalation. Copyright

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