6361-05-3 Usage
Description
(Ethoxycarbonylmethyl)diphenylphosphine, a phosphine compound, is a white to off-white solid with a molecular formula C17H19O3P. It is known for its versatile reactivity and diverse synthetic utility, making it a valuable compound in the field of chemical research and development.
Uses
Used in Organic Synthesis:
(Ethoxycarbonylmethyl)diphenylphosphine is used as a reagent for the formation of carbon-phosphorus bonds in organic synthesis. Its unique properties allow for the creation of new chemical structures and compounds.
Used in Metal-Catalyzed Reactions:
As an effective ligand, (ethoxycarbonylmethyl)diphenylphosphine plays a crucial role in metal-catalyzed reactions, enhancing the efficiency and selectivity of these processes.
Used in Pharmaceutical and Agrochemical Synthesis:
(Ethoxycarbonylmethyl)diphenylphosphine is utilized in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products.
Used in Chemical Research and Development:
Due to its versatile reactivity and diverse synthetic utility, (ethoxycarbonylmethyl)diphenylphosphine has potential applications in the field of chemical research and development, where it can be employed to explore new chemical pathways and create innovative compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 6361-05-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6361-05:
(6*6)+(5*3)+(4*6)+(3*1)+(2*0)+(1*5)=83
83 % 10 = 3
So 6361-05-3 is a valid CAS Registry Number.
6361-05-3Relevant articles and documents
A SIMPLE VARIANT OF THE MICHAELIS-BECKER PHASE TRANSFER
Bondarenko, N. A.,Rudomino, M. V.,Tsvetkov, E. N.
, p. 1076 (1990)
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New Tridentate Carbamoylmethylphosphine Oxides: Synthesis and NMR Spectra
Bondarenko,Belus’,Artyushin,Peregudov
, p. 2273 - 2280 (2021/02/12)
Abstract: Amidation of diphenylphosphorylacetic acid gave tridentate ligands Ph2P(O)CH2CON(R)· CH2CH2P(O)Ph2 (R = Me, Bu, Oct) containing a phosphoryl group in the amide moiety. According to the
Palladium-catalyzed C(sp3)–P(III) bond formation reaction with acylphosphines as phosphorus source
Zhang, Mengyue,Ma, Zhichao,Du, Hongguang,Wang, Zhiqian
, (2020/06/29)
Palladium-catalyzed C(sp3)–P(III) bond formation reaction for alkyl substituted phosphines preparation was developed. In this reaction, various alkyl bromides and limited alkyl chlorides reacted with acylphosphine under relative mild and easily accessible condition, and differential phosphines were afforded in good yields. This reaction made up the application of palladium catalysis in C(sp3)–P(III) bond formation, and indicated a practical application of acylphosphine as a phosphination reagent.
