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BIS(3-aminophenyl) 3,5-di(trifluoromethyl)phenyl phosphine oxide, with the chemical formula C23H16F6N2OP, is a phosphine oxide derivative characterized by its unique structure that includes both phosphine and phenyl groups. BIS(3-AMINOPHENYL) 3,5-DI(TRIFLUOROMETHYL)PHENYL PHOSPHINE OXIDE is known for its ability to coordinate with transition metal ions, such as palladium, and is widely used in various catalytic processes, particularly in the field of transition metal-catalyzed reactions. The presence of trifluoromethyl groups on the phenyl ring imparts distinctive electronic and steric properties, enhancing its utility in synthetic chemistry.

299176-31-1

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299176-31-1 Usage

Uses

Used in Chemical Catalysis:
BIS(3-aminophenyl) 3,5-di(trifluoromethyl)phenyl phosphine oxide is used as a ligand in chemical catalysis for its ability to coordinate with transition metal ions, facilitating a broad spectrum of organic transformations. Its unique structure and the presence of trifluoromethyl groups contribute to its effectiveness in catalytic processes.
Used in Transition Metal-Catalyzed Reactions:
In the field of transition metal-catalyzed reactions, BIS(3-aminophenyl) 3,5-di(trifluoromethyl)phenyl phosphine oxide is used as a ligand to enhance the reactivity and selectivity of the reactions. Its coordination with metals like palladium allows for efficient catalysis in various organic synthesis applications.
Used in Synthetic Chemistry:
BIS(3-aminophenyl) 3,5-di(trifluoromethyl)phenyl phosphine oxide is utilized in synthetic chemistry as a versatile tool for a wide range of chemical reactions. Its structural features make it a valuable asset in the synthesis of complex organic molecules and compounds.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its role in catalytic processes and synthetic chemistry, BIS(3-aminophenyl) 3,5-di(trifluoromethyl)phenyl phosphine oxide could potentially be used in the pharmaceutical industry for the synthesis of complex drug molecules, leveraging its catalytic properties to streamline the production of medicinal compounds.
Used in Material Science:
Similarly, while not specified in the materials, the compound's unique properties might also find applications in material science, where it could be employed in the development of new materials with specific electronic or steric characteristics, thanks to its trifluoromethyl groups and its ability to participate in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 299176-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,1,7 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 299176-31:
(8*2)+(7*9)+(6*9)+(5*1)+(4*7)+(3*6)+(2*3)+(1*1)=191
191 % 10 = 1
So 299176-31-1 is a valid CAS Registry Number.

299176-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(3-aminophenyl)-[3,5-bis(trifluoromethyl)phenyl]phosphoryl]aniline

1.2 Other means of identification

Product number -
Other names N533

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:299176-31-1 SDS

299176-31-1Upstream product

299176-31-1Downstream Products

299176-31-1Relevant academic research and scientific papers

Triarylphosphine oxide derivatives containing fluorine substituents

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Example 3, (2010/01/30)

The invention relates to triarylphosphine oxide derivatives containing fluorine substituents that are useful as a monomer in preparation of polymers with improved properties such as chemical resistance and electrical insulating property as well as adhesiveness and flame retardancy. The triarylphosphine oxide derivatives containing fluorine substituents are represented by the chemical formula1: wherein R1and R2are independently a fluorine-substituted alkyl group; and X is hydrogen, a nitro group, or an amine group.

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