75378-49-3 Usage
Description
Ethyl 4-Phosphanobenzoate is an organic compound that features a phosphorus atom bonded to a benzoate group. It is known for its unique chemical properties and potential applications in various fields due to its ability to undergo specific chemical reactions.
Uses
Used in Chemical Synthesis:
Ethyl 4-Phosphanobenzoate is used as a reagent in the oxidative Heck-Type reaction, which involves the cleavage of a carbon-phosphorus bond of arylphosphonic acids. This reaction is significant in the synthesis of various organic compounds and pharmaceuticals, as it allows for the formation of new carbon-carbon or carbon-heteroatom bonds, expanding the structural diversity of the resulting molecules.
Used in Pharmaceutical Industry:
Ethyl 4-Phosphanobenzoate is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Material Science:
Ethyl 4-Phosphanobenzoate can be utilized in the development of novel materials with specific properties, such as improved thermal stability or enhanced electrical conductivity. Its incorporation into polymers or other materials can lead to the creation of advanced materials for various applications, including electronics, aerospace, and automotive industries.
Check Digit Verification of cas no
The CAS Registry Mumber 75378-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,7 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75378-49:
(7*7)+(6*5)+(5*3)+(4*7)+(3*8)+(2*4)+(1*9)=163
163 % 10 = 3
So 75378-49-3 is a valid CAS Registry Number.
75378-49-3Relevant articles and documents
Oxidative heck-type reaction involving cleavage of a carbon-phosphorus bond of arylphosphonic acids
Inoue, Atsushi,Shinokubo, Hiroshi,Oshima, Koichiro
, p. 1484 - 1485 (2007/10/03)
Cleavage of a carbon-phosphorus bond is achieved under palladium catalysis in an oxidative Heck-type reaction which exploits arylphosphonic acids. The reaction of arylphosphonic acids with alkenes provides arylation products in good yields in the presence of TBAF with trimethylamine oxide as an oxidant. Copyright
