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Diethyl 4-nitrobenzoyl phosphonate is an organic compound with the chemical formula C11H14NO5P. It is a colorless to pale yellow liquid and is soluble in organic solvents. diethyl 4-nitrobenzoyl phosphonate is a derivative of phosphonic acid, featuring a 4-nitrobenzoyl group attached to a phosphonate moiety. It is synthesized by the reaction of diethyl phosphite with 4-nitrobenzoyl chloride. Diethyl 4-nitrobenzoyl phosphonate is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry.

2942-55-4

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2942-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2942-55-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2942-55:
(6*2)+(5*9)+(4*4)+(3*2)+(2*5)+(1*5)=94
94 % 10 = 4
So 2942-55-4 is a valid CAS Registry Number.

2942-55-4Downstream Products

2942-55-4Relevant academic research and scientific papers

Preparation of α-ketophosphonates by oxidation of α-hydroxyphosphonates with chromium-based oxidants

Firouzabadi, Habib,Iranpoor, Nasser,Sobhani, Sara

, p. 1463 - 1471 (2004)

Various types of diethyl α-hydroxyphosphonates were efficiently converted to diethyl α-ketophosphonates by nicotinium dichromate (NDC), nicotinium chlorochromate (NCC), and isonicotinium dichromate (INDC) in high yields.

Preparation of α-ketophosphonates by oxidation of α-hydroxyphosphonates with Pyridinium Chlorochromate (PCC)

Firouzabadi, Habib,Iranpoor, Nasser,Sobhani, Sara

, p. 1483 - 1491 (2007/10/03)

Various types of diethyl α-hydroxyphosphonates were converted efficiently to their corresponding diethyl α-ketophosphonates by pyridiinum chlorochromate (PCC) without cleavage of C(O) - P bond in the absence of solvent or in solution in high yields.

Preparation of α-ketophosphonates by oxidation of α-hydroxyphosphonates with neutral alumina supported potassium permanganate (NASPP) under solvent-free conditions and potassium permanganate in dry benzene

Firouzabadi, Habib,Iranpoor, Nasser,Sobhani, Sara

, p. 477 - 480 (2007/10/03)

Various types of α-hydroxyphosphonates were converted to α-ketophosphonates in high yields by potassium permanganate in dry benzene or by neutral alumina supported potassium permanganate (NASPP) under solvent-free conditions.

High yield preparation of α-ketophosphonates by oxidation of α-hydroxyphosphonates with zinc dichromate trihydrate (ZnCr2O7·3H2O) under solvent-free conditions

Firouzabadi, Habib,Iranpoor, Nasser,Sobhani, Sara,Sardarian, Ali-Reza

, p. 4369 - 4371 (2007/10/03)

Various types of α-hydroxyphosphonates were converted to α-ketophosphonates by zinc dichromate trihydrate in high yields and rates under solvent-free conditions.

A convenient and mild procedure for the preparation of α-keto phosphonates of 1-hydroxyphosphonates under solvent-free conditions using microwave

Kaboudin,Nazari

, p. 2245 - 2250 (2007/10/03)

The Reactions of 1-hydroxyphosphonates on the alumina-supported CrO3 are accelerated by microwave irradiation under solvent-free conditions to afford a high yielding synthesis of α-keto phosphonates.

Surface-mediated solid-phase reactions: The preparation of acyl phosphonates by oxidation of 1-hydroxyphosphonates on the solid surface

Kaboudin, Babak

, p. 3169 - 3171 (2007/10/03)

Alumina-supported CrO3, under solvent-free conditions, was found to be an efficient oxidizing reagent for the preparation of acyl phosphonates from 1-hydroxyphosphonates. This method is an easy, rapid, and high-yielding reaction for the prepara

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