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(4-Methoxyphenyl)phosphinic acid is an organic compound with the chemical formula C7H9O3P. It is a derivative of phosphinic acid, featuring a 4-methoxyphenyl group attached to the phosphorus atom. (4-methoxyphenyl)phosphinic acid is a white crystalline solid and is soluble in organic solvents. It is used as a building block in the synthesis of various phosphorus-containing compounds, such as phosphonates and phosphinates, which have applications in pharmaceuticals, agrochemicals, and materials science. The compound is also known for its potential use as a ligand in coordination chemistry.

53534-65-9

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53534-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53534-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,3 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53534-65:
(7*5)+(6*3)+(5*5)+(4*3)+(3*4)+(2*6)+(1*5)=119
119 % 10 = 9
So 53534-65-9 is a valid CAS Registry Number.

53534-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxyphenyl)phosphinic acid

1.2 Other means of identification

Product number -
Other names 4-methoxy-phenylphosphinic 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:53534-65-9 SDS

53534-65-9Downstream Products

53534-65-9Relevant academic research and scientific papers

Recent advances in phosphorus-carbon bond formation: Synthesis of H-phosphinic acid derivatives from hypophosphorous compounds

Montchamp, Jean-Luc

, p. 2388 - 2406 (2007/10/03)

This account summarizes the research conducted in our laboratory over the past five years. New methodologies were devised for the formation of P-C bonds with a focus on the reactions of hypophosphorous acid derivatives. Three types of reactions have been developed: palladium-catalyzed cross-coupling, room-temperature radical addition, and palladium-catalyzed addition. Our results are summarized in each of these areas and include some of our most recent data. (1) Our palladium-catalyzed cross-coupling has been extended to the direct coupling of alkyl phosphinates with a variety of aryl, heteroaryl, and even alkenyl electrophiles. (2) The addition of sodium hypophosphite under radical conditions is extended from alkenes to alkynes. (3) The catalytic addition of hypophosphorous compounds using palladium catalysts (hydrophosphinylation) is also discussed.

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