1831-63-6

Basic information

• Product Name: CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE
• Synonyms: CARBOXYMETHYLDIPHENYLPHOSPHINE;CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE;Carboxymethyl diphenylphosphine oxide, 98 %;2-(Diphenylphosphino)acetic acid;Diphenylphosphinoacetic acid;2-di(phenyl)phosphorylethanoic acid;[Bis(phenyl)phosphoryl]acetic acid;Bisphenyl(carboxymethyl)phosphine oxide
• CAS NO: 1831-63-6
• Molecular Formula: C₁₄H₁₃O₃P
• Molecular Weight: 244.23
• Mol File: 1831-63-6.mol
• Article Data: 9

Chemical Properties

• Melting Point: 145-146 °C
• Boiling Point: 419.1°Cat760mmHg
• Flash Point: 207.3°C
• Appearance: /
• Density: 1.27g/cm³
• Vapor Pressure: 8.95E-08mmHg at 25°C
• Refractive Index: 1.593
• PKA: 3.73±0.10(Predicted)
• CAS DataBase Reference: CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE(1831-63-6)
• EPA Substance Registry System: CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE(1831-63-6)

Safety Data

• Hazardous Substances Data: 1831-63-6(Hazardous Substances Data)

Usage

General Description

CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE is a chemical compound with the molecular formula C14H13O3P. It is a phosphorous-based compound that contains both a carboxymethyl and a diphenyl group. CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE is commonly used in organic and inorganic chemical reactions as a ligand and as a catalyst. It has shown potential in promoting various chemical reactions, including the formation of carbon-carbon and carbon-heteroatom bonds. Additionally, it has been studied for its potential applications in the synthesis of pharmaceuticals and other fine chemicals. Overall, CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE has practical utility as a versatile reagent in organic chemistry.

InChI:InChI=1/C14H13O3P/c15-14(16)11-18(17,12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10H,11H2,(H,15,16)

Upstream product

• 79-11-8 chloroacetic acid 
• 4559-70-0 Diphenylphosphine oxide 
• 24630-80-6 diphenylphosphine oxide 
• 96-34-4 methyl chloroacetate 
• 829-85-6 diphenylphosphane 
• 1706-91-8 isopropyl diphenylphosphinate 
• 6361-05-3 ethyl 2-(diphenylphosphoryl)acetate 
• 124-38-9 carbon dioxide 
• 2129-89-7 diphenyl(methyl)phosphine oxide 
• 2741-38-0 allyldiphenylphosphine 
• 114034-73-0 Diphenyl-di-carbaethoxymethyl-phosphonium-bromid 

Downstream Products

• 6361-05-3 ethyl 2-(diphenylphosphoryl)acetate 
• 21993-16-8 carbomethoxymethylenediphenylphosphine oxide 
• 2129-89-7 diphenyl(methyl)phosphine oxide 
• 97937-88-7 2-(diphenyl-phosphinoyl)-N,N-diisobutyl-acetamide 
• 259085-57-9 2-(diphenyl-phosphinoyl)-N,N-dihexyl-acetamide 
• 80413-42-9 oxide of diphenylphosphite 
• 80413-41-8 oxide of diphenylphosphite 
• 1000670-09-6 diphenylphosphorylacetic acid chloride 

Relevant articles and documents

2-Diphenylphosphinonyl-acetyl as a Remote Directing Group for the Highly Stereoselective Synthesis of β-Glycosides

The configuration of the anomeric glycosidic linkages is crucial for maintaining the biological functions and activities of carbohydrate molecules. However, their stereochemistry control in glycosylation represents one of the most challenging tasks in car

Synthesis and characterisation of new molybdenum - oxo complexes containing diphenylphosphinylacetic acid and 2-(tert-butylsulphoxide)phenyldiphenylphosphine oxide as bidentate ligands

Reaction of the ligands diphenylphosphinylacetic acid Ph2P(O)CH2COOH (1) and 2-(tert-butylthio)phenyldiphenylphosphine oxide Ph2P(O)C6H4tBuS (2) with "MoO2Cl2", result

Complex formation of some carbamoylmethylphosphine oxides and methylenediphosphine dioxides with alkali metal cations. The "anomalous aryl enhancement" effect

Conductometry in anhydrous hexane at 25°C was used to measure the stability constants of alkali cation complexes of a series of N,N-diethylcarbamoylmethylphosphine oxides and methylenediphosphine dioxides. The "anomalous aryl enhancement" effect is the strongest in the complexes with tetraphenyldiphosphine dioxide.