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2,4,4-triphenyl-4H-1,4-benzoxaphosphinin-4-ium is a phosphorus-containing organic compound characterized by a complex molecular structure with three phenyl groups attached to a central phosphorus atom. This cationic species is known for its unique reactivity and potential in synthetic chemistry, making it a valuable tool in various applications.

72596-47-5

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72596-47-5 Usage

Uses

Used in Organic Synthesis:
2,4,4-triphenyl-4H-1,4-benzoxaphosphinin-4-ium is used as a catalyst in organic synthesis for its ability to facilitate various chemical reactions, enhancing the efficiency and selectivity of the processes.
Used in Catalysis Reactions:
In the field of catalysis, 2,4,4-triphenyl-4H-1,4-benzoxaphosphinin-4-ium is utilized as a catalyst to accelerate reaction rates and improve the yield of desired products, making it a key component in many chemical processes.
Used in the Development of New Materials:
2,4,4-triphenyl-4H-1,4-benzoxaphosphinin-4-ium is employed in the research and development of innovative materials, leveraging its unique structure and reactivity to create novel compounds with specific properties for various applications.
Used in Pharmaceutical Development:
2,4,4-triphenyl-4H-1,4-benzoxaphosphinin-4-ium is also used in the pharmaceutical industry as a catalyst or intermediate in the synthesis of new drugs, contributing to the discovery and production of potential therapeutic agents.
Used in Chemical Research:
2,4,4-triphenyl-4H-1,4-benzoxaphosphinin-4-ium serves as a subject of study in chemical research, where its properties and reactivity are explored to gain insights into new reaction mechanisms and to develop new synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 72596-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,9 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72596-47:
(7*7)+(6*2)+(5*5)+(4*9)+(3*6)+(2*4)+(1*7)=155
155 % 10 = 5
So 72596-47-5 is a valid CAS Registry Number.

72596-47-5SDS

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 2,4,4-triphenyl-1,4-benzoxaphosphinin-4-ium,bromide

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72596-47-5 SDS

72596-47-5Downstream Products

72596-47-5Relevant academic research and scientific papers

Pd(0)-Catalyzed Intramolecular "ylide-Ullmann-Type" Cyclization of Carbonyl-Stabilized Phosphonium Ylides and Access to Phosphachromones by Exocyclic P-C Cleavage

Xu, Shuangshuang,Huang, Haiyang,Yan, Zeen,Xiao, Qiang

, p. 10018 - 10022 (2019)

An unprecedented palladium-catalyzed intramolecular Ullmann-type cyclization of carbonyl-stabilized phosphonium ylides with aryl bromides was successfully developed. Furthermore, a base-promoted chemoselective hydrolysis of exocyclic P-C bond of the corresponding phosphonium salts delivered various phosphachromones. Excellent selectivity and high efficiency and good functional group tolerance were observed.

Method for synthesizing phosphorus mixed color orthoketone derivative

-

Paragraph 0017, (2019/06/07)

The invention discloses a method for synthesizing a phosphorus mixed color orthoketone derivative. The method comprises the following steps: taking 2'-phenyl halogenate-beta-carbonyl phosphorus ylideas a raw material, sufficiently dissolving the raw mater

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