Diphenyl phosphite - CAS 4712-55-4

Catalog:	BB026223
Product Name:	Diphenyl phosphite
CAS:	4712-55-4
Synonyms:	oxo(diphenoxy)phosphanium

Technical Data

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Computed Properties

IUPAC Name:	oxo(diphenoxy)phosphanium
Description:	Diphenyl phosphite (CAS# 4712-55-4) is a reactant used in the synthesis of α-hydroxyphosphonates and α-hydroxyphosphinates for their antioxidant and antimicrobial activity.
Molecular Weight:	234.19
Molecular Formula:	C12H10O3P+
Canonical SMILES:	C1=CC=C(C=C1)O[P+](=O)OC2=CC=CC=C2
InChI:	InChI=1S/C12H10O3P/c13-16(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H/q+1
InChI Key:	CDXVUROVRIFQMV-UHFFFAOYSA-N
Boiling Point:	218-219 °C / 26 mmHg (lit.)
Density:	1.223 g/cm³
Appearance:	Light visous liquid
LogP:	3.53410

Publication Number	Title	Priority Date
CN-112829414-A	Composite light diffusion plate and preparation method thereof	20201231
CN-112280405-A	Water-based halogen-free intumescent flame-retardant coating adhesive, preparation method and flame-retardant fabric made of coating adhesive	20201109
CN-112175002-A	Method for auxiliary synthesis of anti-SARS octapeptide by TDPBP derived carrier	20201009
CN-111848670-A	Preparation method of high-purity cardanol phosphate	20200810
CN-113359391-A	Photoresist composition and method for forming photoresist pattern	20200618

PMID	Publication Date	Title	Journal
33049310	20210401	Evaluation of a multiplexed, multispecies nuclear receptor assay for chemical hazard assessment	Toxicology in vitro : an international journal published in association with BIBRA
29442501	20180308	Exploiting the S4-S5 Specificity of Human Neutrophil Proteinase 3 to Improve the Potency of Peptidyl Di(chlorophenyl)-phosphonate Ester Inhibitors: A Kinetic and Molecular Modeling Analysis	Journal of medicinal chemistry
22967814	20121201	Chymotrypsin-like serine proteinases are involved in the maintenance of cell viability	Biochimie
22658243	20121001	Structural and anticancer properties of hydrogen bonded diphenyl phosphate adducts of Pt(IV) complexes: the importance of pKa matching	Journal of inorganic biochemistry
22388950	20120414	A novel ketone olefination via organozinc reagents in the presence of diphenyl phosphite	Organic & biomolecular chemistry

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Related Functional Groups

Phosphorus Compounds

[169689-05-8]
1S,2S-DHAC-Phenyl Trost Ligand
[124755-24-4]
Ethyl [bis(2,2,2-trifluoroethoxy)phosphinyl]acetate
[28845-75-2]
Ethyl 2,2-dibromodiethylphosphonoacetate
[1536463-79-2]
Ethyl 2-dibutoxyphosphorylbutanoate
[26342-16-5]
ethyl 3-(diethoxyphosphoryl)benzoate
[719-80-2]
Ethyl diphenylphosphinite

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GHS Hazard Statement:	H302 (97.09%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P264, P270, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, and P501
Signal Word:	Warning

Complexity:	198
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	233.03675617
Formal Charge:	1
Heavy Atom Count:	16
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	233.03675617
Rotatable Bond Count:	4
Topological Polar Surface Area:	35.5 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	3.1