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(4-Trifluoromethylphenyl)phosphine, with the molecular formula C7H5F3P, is a phosphine derivative characterized by the attachment of a trifluoromethylphenyl group to a phosphorus atom. (4-TRIFLUOROMETHYLPHENYL)PHOSPHINE is known for its applications in organometallic chemistry and catalysis, where it serves as a versatile ligand capable of bonding with transition metal ions to catalyze a range of chemical reactions. Additionally, it is utilized as a reagent in the synthesis of various organic compounds, making it a valuable asset in the field of chemical research and development.

473808-83-2

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473808-83-2 Usage

Uses

Used in Organometallic Chemistry:
(4-Trifluoromethylphenyl)phosphine is used as a ligand for [enhancing the reactivity and selectivity of transition metal catalysts] because of its ability to bond with transition metal ions, thereby facilitating various chemical reactions.
Used in Catalysis:
In the field of catalysis, (4-Trifluoromethylphenyl)phosphine is used as a catalyst component for [improving the efficiency of chemical reactions] due to its capacity to modify the properties of transition metal catalysts.
Used in the Synthesis of Organic Compounds:
(4-Trifluoromethylphenyl)phosphine is utilized as a reagent in organic synthesis for [enabling the formation of desired organic products] through its participation in various chemical reactions.
Used in Pharmaceutical and Agrochemical Industries:
Although not explicitly mentioned in the provided materials, given its role in organometallic chemistry and catalysis, (4-Trifluoromethylphenyl)phosphine may also be used in the pharmaceutical and agrochemical industries for [the development of new drugs and agrochemicals], given the importance of organometallic compounds and catalysts in the synthesis of complex organic molecules.
Safety Note:
It is important to handle (4-Trifluoromethylphenyl)phosphine with care in a controlled laboratory environment due to its potentially hazardous nature. Proper safety measures should be implemented to ensure the well-being of researchers and the integrity of the experiments.

Check Digit Verification of cas no

The CAS Registry Mumber 473808-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,8,0 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 473808-83:
(8*4)+(7*7)+(6*3)+(5*8)+(4*0)+(3*8)+(2*8)+(1*3)=182
182 % 10 = 2
So 473808-83-2 is a valid CAS Registry Number.

473808-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(trifluoromethyl)phenyl]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:473808-83-2 SDS

473808-83-2Downstream Products

473808-83-2Relevant academic research and scientific papers

Reversing the Tradeoff between Rate and Overpotential in Molecular Electrocatalysts for H2 Production

Klug, Christina M.,Cardenas, Allan Jay P.,Morris Bullock,O'Hagan, Molly,Wiedner, Eric S.

, p. 3286 - 3296 (2018/04/14)

A longstanding challenge in molecular electrocatalysis is to design catalysts that break away from the tradeoff between rate and overpotential arising from electronic scaling relationships. Here we report an inversion of the rate-overpotential correlation

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