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CIS,CIS,CIS-TETRAKIS(DIPHENYLPHOSPHINOMETHYL)CYCLOPENTANE is a complex organic compound that features a cyclopentane ring with four diphenylphosphinomethyl groups attached in a cis configuration. As a member of the phosphine ligand family, it is widely utilized in coordination chemistry for its chelating properties, enabling it to bind with metal ions effectively. CIS,CIS,CIS-TETRAKIS(DIPHENYLPHOSPHINOMETHYL)CYCLOPENTANE's significant steric hindrance, due to the bulky diphenylphosphinomethyl groups, makes it a potent agent in blocking reaction sites or providing steric protection in metal-catalyzed reactions. Its unique structure and properties render it a valuable asset in the realms of organic synthesis and catalytic processes, with its specific stereochemistry and chelating ability attracting interest in coordination chemistry and materials science.

333380-86-2

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333380-86-2 Usage

Uses

Used in Coordination Chemistry:
CIS,CIS,CIS-TETRAKIS(DIPHENYLPHOSPHINOMETHYL)CYCLOPENTANE is used as a chelating agent for [its ability to bind with metal ions], which is crucial in the study and application of coordination compounds.
Used in Organic Synthesis:
In the field of Organic Synthesis, CIS,CIS,CIS-TETRAKIS(DIPHENYLPHOSPHINOMETHYL)CYCLOPENTANE is used as a steric protection agent for [its capacity to block reaction sites], facilitating the synthesis of complex organic molecules.
Used in Catalytic Processes:
CIS,CIS,CIS-TETRAKIS(DIPHENYLPHOSPHINOMETHYL)CYCLOPENTANE is utilized as a ligand in Catalytic Processes for [its role in enhancing the selectivity and efficiency of catalytic reactions], particularly in metal-catalyzed transformations.
Used in Materials Science:
In Materials Science, CIS,CIS,CIS-TETRAKIS(DIPHENYLPHOSPHINOMETHYL)CYCLOPENTANE is employed as a structural component for [its contribution to the development of new materials with unique properties], owing to its specific stereochemistry and chelating ability.

Check Digit Verification of cas no

The CAS Registry Mumber 333380-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,8 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 333380-86:
(8*3)+(7*3)+(6*3)+(5*3)+(4*8)+(3*0)+(2*8)+(1*6)=132
132 % 10 = 2
So 333380-86-2 is a valid CAS Registry Number.

333380-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenyl-[[(1S,2S,3R,4R)-2,3,4-tris(diphenylphosphanylmethyl)cyclopentyl]methyl]phosphane

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:333380-86-2 SDS

333380-86-2Downstream Products

333380-86-2Relevant academic research and scientific papers

A new tetratertiary phosphine ligand and its use in Pd-catalyzed allylic substitution

Laurenti,Feuerstein,Pepe,Doucet,Santelli

, p. 1633 - 1637 (2007/10/03)

A new tetraphosphine, the cis-cis-cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)cyclopentane (Tedicyp) 1 has been synthesized, characterized, and used in Pd-catalyzed allylic substitutions. The Tedicyp was easily prepared in seven steps from the commercially available himic anhydride. The structure of the complex Tedicyp-borane was determined by X-ray analysis. The tetraphosphine in combination with [Pd(η3-C3H5)Cl]2 affords a very efficient catalyst for allylic substitution of several allylic acetates. Under mild conditions, very high turnover numbers and turnover frequencies have been obtained.

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