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(2-iodophenyl)phenylphosphinic acid is a phosphinic acid derivative with the molecular formula C12H10IO2P. It is a white to off-white solid that is insoluble in water.

5435-79-0

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5435-79-0 Usage

Uses

Used in Organic Synthesis:
(2-iodophenyl)phenylphosphinic acid is used as a ligand for enhancing the efficiency and selectivity of various organic reactions.
Used in Catalysis:
(2-iodophenyl)phenylphosphinic acid is used as a ligand in catalytic processes to improve the catalytic activity and stability of catalysts.
Used in Pharmaceutical Industry:
(2-iodophenyl)phenylphosphinic acid is used as a pharmaceutical intermediate, contributing to the development of new drugs and therapeutic agents.
Used in Material Science:
(2-iodophenyl)phenylphosphinic acid is used as a chelating agent in metal ion coordination chemistry, playing a role in the synthesis of new materials with specific properties.
Used as a Reagent:
(2-iodophenyl)phenylphosphinic acid is used as a reagent in organic reactions, facilitating specific transformations and providing access to desired products.
Used in Medicinal Chemistry:
(2-iodophenyl)phenylphosphinic acid has potential biological activity and pharmacological properties, making it a candidate for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5435-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5435-79:
(6*5)+(5*4)+(4*3)+(3*5)+(2*7)+(1*9)=100
100 % 10 = 0
So 5435-79-0 is a valid CAS Registry Number.

5435-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-Jod-phenyl)-phenyl-phosphinsaeure

1.2 Other means of identification

Product number -
Other names Urea,(2-iodophenyl)

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:5435-79-0 SDS

5435-79-0Upstream product

5435-79-0Downstream Products

5435-79-0Relevant academic research and scientific papers

Directed ortho-lithiation of unprotected diphenylphosphinic acids

Ya?ez Rodríguez, Víctor,Del águila, Miguel ángel,Iglesias, María José,López Ortiz, Fernando

experimental part, p. 7355 - 7362 (2012/09/22)

Directed ortho lithiation of diphenylphosphinic acid and subsequent electrophilic trapping provides mono ortho-functionalized derivatives including enantiopure γ-aminophosphinic acids in moderate yields. Copper catalyzed coupling of the ortho anion leads to biphenyl-2,2′- diylbis(phenylphosphinic acid), a phosphorus analogue of biphenyl-2,2′- dicarboxylic acid. Preliminary studies of the metal-binding abilities of this O,O-chelating ligand towards a series of metal cations are included.

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