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4-Chlorophenyl bis(2-pyridyl) phosphate is a chemical compound with the molecular formula C16H12ClNO4P. It is a derivative of phenyl phosphate, featuring a 4-chlorophenyl group and two pyridyl groups attached to the phosphate center. 4-chlorophenyl bis(2-pyridyl) phosphate is known for its potential use as a flame retardant, particularly in polymers and plastics, due to its ability to enhance thermal stability and reduce flammability. It is also of interest in the field of organophosphorus chemistry, where it may be studied for its reactivity and potential applications in various chemical processes. The compound's structure and properties make it a subject of research in material science and chemical engineering.

1659-24-1

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1659-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1659-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1659-24:
(6*1)+(5*6)+(4*5)+(3*9)+(2*2)+(1*4)=91
91 % 10 = 1
So 1659-24-1 is a valid CAS Registry Number.

1659-24-1Downstream Products

1659-24-1Relevant academic research and scientific papers

Activating water: Important effects of non-leaving groups on the hydrolysis of phosphate triesters

Kirby, Anthony J.,Medeiros, Michelle,Oliveira, Pedro S. M.,Orth, Elisa S.,Brandao, Tiago A. S.,Wanderlind, Eduardo H.,Amer, Almahdi,Williams, Nicholas H.,Nome, Faruk

, p. 14996 - 15004 (2012/02/03)

The high rate of spontaneous hydrolysis of tris-2-pyridyl phosphate (TPP) is explained by the activating effects of the non-leaving ("spectator" ) groups on P-OAr cleavage, and not by intramolecular catalysis. Previous work on phosphate-transfer reactions has concentrated on the contributions to reactivity of the nucleophile and the leaving group, but our results make clear that the effects of the non-leaving groups on phosphorus can be equally significant. Rate measurements for three series of phosphate triesters showed that sensitivities to the non-leaving groups are substantial for spontaneous hydrolysis reactions, although significantly smaller for reactions with good nucleophiles. There are clear differences between triaryl and dialkyl aryl triesters in sensitivities to leaving and non-leaving groups with the more reactive triaryl systems showing lower values for both βLG and βNLG. Intramolecular catalysis of the hydrolysis of TPP by the neighbouring pyridine nitrogens is insignificant, primarily because of their low basicity.

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