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(2-Hydroxyphenyl)diphenylphosphine

Catalog Number
ACM60254106-1
Product Name
(2-Hydroxyphenyl)diphenylphosphine
Structure
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CAS
60254-10-6
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Synonyms
(o-Diphenylphosphino)phenol, (2-Diphenylphosphino)phenol, 2-(Diphenylphosphino)phenol, 60254-10-6, (o-Hydroxyphenol)diphenylphosphine, (2-Hydroxyphenyl)diphenylphosphine, 2-diphenylphosphanylphenol, AC1L9OUW, Phenol, 2-(diphenylphosphino)-, CTK2F0990, AKOS016000563, SC11177, AK119092, KB-224055
IUPAC Name
2-diphenylphosphanylphenol
Molecular Weight
278.28
Molecular Formula
C18H15OP
Canonical SMILES
C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3O
InChI
InChI=1S/C18H15OP/c19-17-13-7-8-14-18(17)20(15-9-3-1-4-10-15)16-11-5-2-6-12-16/h1-14,19H;
InChI Key
HGHOYIFINVBZKO-UHFFFAOYSA-N
Purity
96%
Complexity
263
Covalently-Bonded Unit Count
1
Exact Mass
278.08600
H-Bond Acceptor
1
H-Bond Donor
1
Heavy Atom Count
20
Monoisotopic Mass
278.086g/mol
Rotatable Bond Count
3
Topological Polar Surface Area
20.2A^2
Application
(2-Hydroxyphenyl)diphenylphosphine serves as a versatile catalyst with several important applications. It plays a critical role in the preparation of hydroxy(phosphinoxy)biphenyls, facilitating efficient synthesis processes. Additionally, it is instrumental in the formation of ethylene copolymers, enabling the copolymerization of ethylene with linear olefins, which is essential for producing various advanced materials. Furthermore, this compound is used in the silylation of aryl halides, a key reaction in organic chemistry that introduces functional versatility into molecules. These capabilities make (2-Hydroxyphenyl)diphenylphosphine a valuable tool in both industrial and research settings.
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