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Phosphonochloridic acid, ethyl-, ethyl ester, also known as ethyl phosphonochloridate, is an organophosphorus compound with the chemical formula C4H10ClO3P. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 180.55 g/mol. Phosphonochloridic acid, ethyl-, ethyl ester is primarily used as a reagent in the synthesis of various organophosphorus compounds, such as pesticides, flame retardants, and pharmaceuticals. Ethyl phosphonochloridate is also employed as a coupling agent in the production of polymers and as a chlorinating agent in organic synthesis. Due to its reactivity and potential toxicity, it is essential to handle this chemical with proper safety precautions and in accordance with established guidelines.

5284-10-6

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5284-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5284-10-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5284-10:
(6*5)+(5*2)+(4*8)+(3*4)+(2*1)+(1*0)=86
86 % 10 = 6
So 5284-10-6 is a valid CAS Registry Number.

5284-10-6Relevant academic research and scientific papers

Reaction of Trichloro(o-phenylenedioxy)phosphorane with Four-Coordinate Phosphorus Esters

Khusainova,Reshetkova,Cherkasov

, p. 367 - 369 (2007/10/03)

Reactions of trialkyl phosphates and dialkyl alkenylphosphonates with trichloro(o-phenylenedioxy)phosphorane result in selective replacement of one alkoxy group on the phosphorus by a chlorine atom. Alkylphosphonates react with trichloro(o-phenylenedioxy)phosphorane to give alkyl alkylphosphonochloridates as the major products and small amounts of alkylphosphonic dichlorides.

Reaction of Tricoordinate Phosphorus Compounds with Organophosphorus Pseudohalogens. 1. Desulfurization and Deoxygenation of Oxophosphoranesulfenyl Chlorides. Scope and Mechanism

Krawczyk, E.,Mikolajczak, J.,Skowronska, A.,Michalski, J.

, p. 4963 - 4970 (2007/10/02)

The reaction of oxophosphoranesulfenyl chlorides RR'P(O)SCl 2 with PIII compounds has been investigated.Its mechanistic features have been elucidated by variable-temperature 31P NMR spectroscopy and stereochemical changes at PIV and PIII phosphorus centers.These studies show that in all cases phosphonium intermediates containing the sulfur bridge >P(O)-S-P(+)P(S)-O-P(+)-Cl(-).The latter decomposes by the attack of the chloride anion on the thiophosphoryl center (deoxygenation pathway). 31P NMR studies fully corroborated the observed stereochemical changes.

REACTION OF TRICOORDINATE PHOSPHORUS COMPOUNDS WITH PSEUDOHALOGENS. SCOPE AND MECHANISM

Skowronska, Aleksandra,Krawczyk, Ewa,Burski, Janusz

, p. 233 - 236 (2007/10/02)

The selectivity of sulphur, selenium and oxygen removal from pseudohalogens: phosphorus disulphides 1 and 2, diselenides 3 and oxophosphoranesulphenyl chlorides 4 has been investigated.A mechanistic rationalization is proposed to account for sulphur(selenium)/oxygen extrusion variation as a function of substrates structure and reaction conditions.

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