4712-55-4 | Diphenyl phosphite

Packsize	Purity	Availability	Price	Discounted Price
25g	80%	in stock	$12.00	$9.00
100g	80%	in stock	$30.00	$21.00
500g	80%	in stock	$63.00	$44.00

Description

• Catalog Number: AI50773
• Chemical Name: Diphenyl phosphite
• CAS Number: 4712-55-4
• Molecular Formula: C12H11O3P
• Molecular Weight: 234.1877
• MDL Number: MFCD00044497
• SMILES: O=P(Oc1ccccc1)Oc1ccccc1
• NSC Number: 43786

Computed Properties

• Complexity: 198
• Covalently-Bonded Unit Count: 1
• Formal Charge: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• XLogP3: 3.1

Literature

• Chymotrypsin-like serine proteinases are involved in the maintenance of cell viability.

  Biochimie 20121201

• Structural and anticancer properties of hydrogen bonded diphenyl phosphate adducts of Pt(IV) complexes: the importance of pKa matching.

  Journal of inorganic biochemistry 20121001

• [μ-2,3,5,6-Tetra-kis(2-pyrid-yl)pyrazine-κN,N,N:N,N,N]bis-[diaqua(dihydrogen m-phenylene-diphospho-nato-κO)nickel(II)] dihydrate.

  Acta crystallographica. Section E, Structure reports online 20101101

• High-dielectric polymer composite materials from a series of mixed-metal phenylphosphonates, ATi(C6H5PO3)3 for dielectric energy storage.

  ACS applied materials & interfaces 20100901

• Squaramide-catalyzed enantioselective Michael addition of diphenyl phosphite to nitroalkenes.

  Angewandte Chemie (International ed. in English) 20100101

• Enantioselective three-component Kabachnik-Fields reaction catalyzed by chiral scandium(III)-N,N'-dioxide complexes.

  Organic letters 20090319

• Comparison of the structure and magnetic order in a series of layered Ni(II) organophosphonates, Ni[(RPO3)(H2O)] (R = C6H5, CH3, C18H37).

  Inorganic chemistry 20081201

• A convenient and stereoselective synthesis of 11Z-3,4-didehydroretinal by Horner-Emmons reaction using diphenyl phosphonate.

  Chemical & pharmaceutical bulletin 20080101

• Enantioselective 1,4-addition reactions of diphenyl phosphite to nitroalkenes catalyzed by an axially chiral guanidine.

  Journal of the American Chemical Society 20071121

• Determination of impurities in flame retardant monomer 2-carboxyl ethyl(phenyl) phosphinic acid by ion chromotography.

  Journal of chromatography. A 20070629

• Galactose-derived phosphonate analogues as potential inhibitors of phosphatidylinositol biosynthesis in mycobacteria.

  Organic & biomolecular chemistry 20070321

• Diphenyl phosphonate inhibitors for the urokinase-type plasminogen activator: optimization of the P4 position.

  Journal of medicinal chemistry 20060921

• ESI-FTICR mass spectrometric study of alcohol complexation properties of mono- and diphosphonate-bridged cavitands.

  Journal of the American Society for Mass Spectrometry 20060201

• Synthesis of sterically hindered peptide analogs using diphenyl phosphite as the coupling reagent.

  Bioorganic chemistry 20051001

• Development of irreversible diphenyl phosphonate inhibitors for urokinase plasminogen activator.

  Journal of medicinal chemistry 20040506