Welcome to LookChem.com Sign In|Join Free
  • or
CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1831-63-6

Post Buying Request

1831-63-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1831-63-6 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.

Check Digit Verification of cas no

The CAS Registry Mumber 1831-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1831-63:
(6*1)+(5*8)+(4*3)+(3*1)+(2*6)+(1*3)=76
76 % 10 = 6
So 1831-63-6 is a valid CAS Registry Number.
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)

1831-63-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-diphenylphosphorylacetic acid

1.2 Other means of identification

Product number -
Other names diphenylphosphinoylacetic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1831-63-6 SDS

1831-63-6Relevant academic research and scientific papers

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

Liu, Xianglai,Lin, Yetong,Liu, Ao,Sun, Qianhui,Sun, Huiyong,Xu, Peng,Li, Guolong,Song, Yingying,Xie, Weijia,Sun, Haopeng,Yu, Biao,Li, Wei

supporting information, p. 443 - 452 (2021/12/27)

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

Knoevenagel Condensation of Phosphinoylacetic Acids with Aldehydes: An Efficient One-Pot Strategy for the Synthesis of P-Functionalized Alkenyl Compounds

Dziuba, Kamil,Frynas, S?awomir,Szwaczko, Katarzyna

, p. 2142 - 2154 (2021/01/21)

A wide range of commercially available aldehydes have been applied to Knoevenagel condensation reaction to give E -alkenylphosphine oxides and vinylphosphine oxides. The readily available phosphinoylacetic acids derived from P(O)-H compounds were used as the starting materials in the reaction, providing a highly stereoselective and efficient method for constructing α,β-unsaturated phosphine oxides. Moreover, this simple and practical procedure provides an alternative and more environmentally friendly synthesis strategy for this type of P-functionalized alkenyl compounds.

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

Buchweitz, Maria,Luck, Rudy L.,Sreehari, Soumya,Beganskiene, Aldona,Urnezius, Eugenijus

experimental part, p. 1818 - 1822 (2010/09/04)

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

Sequestration, fluorometric detection, and mass spectroscopy analysis of lanthanide ions using surface modified magnetic microspheres for microfluidic manipulation

Shkrob, Ilya A.,Kaminski, Michael D.,Mertz, Carol J.,Rickert, Paul G.,Derzon, Mark S.,Rahimian, Kamyar

supporting information; experimental part, p. 15705 - 15710 (2010/01/30)

Several methods for rapid sequestration, fluorometric detection, and the subsequent mass spectroscopic analysis of lanthanide ions using surface modified polystyrene magnetic microspheres are demonstrated. Mixed-ligand antenna complexes of Eu3+ in which one of the ligands is attached to the surface of the microspheres have been used as a means for the sequestration, immobilization, and detection of these ions. Using the ion-exchange properties of these microspheres, this scheme has been extended to the detection of nonluminescent ions. The principles of these assays form the basis for operation of a portable microfluidic device for general analytical and nuclear forensics applications and indicate the manner in which the established methods of analytical chemistry, such as liquid-liquid extraction and ion-exchange chromatography, can be adapted for such miniature devices.

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

Evreinov,Safronova,Yarkevich,Kharitonov,Bondarenko,Tsvetkov

, p. 1047 - 1051 (2007/10/03)

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.

Calixarenes with diphenylphosphoryl acetamide functions at the upper rim. A new class of highly efficient extractants for lanthanides and actinides

Arnaud-Neu, Francoise,Boehmer, Volker,Dozol, Jean-Francois,Gruettner, Cordula,Jakobi, Ralf A.,Kraft, Dagmar,Mauprivez, Olivier,Rouquette, Helene,Schwing-Weill, Marie-Jose,Simon, Nicole,Vogt, Walter

, p. 1175 - 1182 (2007/10/03)

Various calix[4]arene tetraalkyl ethers and a calix[5]arene pentaalkyl ether substituted at the upper rim by the CMPO-like functional group -NH-C(O)-CH2-P(O)Ph2 as well as some linear model compounds have been synthesized for the fir

ALKYLATION REACTIONS OF DIALKYL HYDROGEN PHOSPHITES AND DIARYLPHOSPHINE OXIDES UNDER PHASE-TRANSFER CONDITIONS

Petrov, K. A.,Sivova, L. I.,Smirnov, I. V.,Kryukova, L. Yu.

, p. 264 - 268 (2007/10/02)

It was shown that phosphonates and tertiary phosphine oxides can be synthesized by the alkylation of acid phosphites and diarylphosphine oxides in a nonpolar solvent in presence of solid potassium hydroxide and potassium carbonate and also catalytic amounts of 18-crown ether (or in its absence). (Diarylphosphinyl)methyl ethers of mono- and oligo-etylene glycols were synthesized by the reactions of diaryl(chloromethyl)phosphine oxides with lithium glycolates

A Simple Synthesis and Some Synthetic Applications of Substituted Phosphide and Phosphinite Anions

Tsvetkov, E. N.,Bondarenko, N. A.,Malakhova, I. G.,Kabachnik, M. I.

, p. 198 - 208 (2007/10/02)

Based on data for the acidity relationship of phosphines and phosphinous acids and water in dimethyl sulfoxide and water, a simple method is reported for the generation of phosphide and phosphinite anions by the action of concentrated aqueous alkali on primary and secondary phosphines as well as phosphinous acids in dimethyl sulfoxide or other dipolar aprotic solvents.Alkylation of the anion yields secondary and tertiary phosphines, polyphosphines, functionally substituted phosphines as well as similarly substituted phosphine oxides.Phosphinous acids have beenalkylated in various solvents in two-phase systems containing concentrated aqueous alkali and tetrabutylammonium iodide as phase transfer catalyst.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1831-63-6