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Diphenyl isopropylphosphoramidate, also known as DFP, is a potent organophosphorus compound that acts as an irreversible inhibitor of acetylcholinesterase, an enzyme responsible for breaking down the neurotransmitter acetylcholine. This inhibition leads to the accumulation of acetylcholine in the synaptic cleft, causing overstimulation of the nervous system. DFP is a colorless, oily liquid with a slight odor and is highly toxic, posing a significant risk to human health through inhalation, ingestion, or skin contact. It has been historically used as a chemical warfare agent and as an insecticide, but its use has been largely discontinued due to its extreme toxicity and potential for misuse.

5756-04-7

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5756-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5756-04-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5756-04:
(6*5)+(5*7)+(4*5)+(3*6)+(2*0)+(1*4)=107
107 % 10 = 7
So 5756-04-7 is a valid CAS Registry Number.

5756-04-7Relevant academic research and scientific papers

O -Phthalaldehyde catalyzed hydrolysis of organophosphinic amides and other P(O)-NH containing compounds

Li, Bin-Jie,Simard, Ryan D.,Beauchemin, André M.

, p. 8667 - 8670 (2017)

Over 50 years ago, Jencks and Gilchrist showed that formaldehyde catalyses the hydrolysis of phosphoramidate through electrophilic activation, induced by covalent attachment to its nitrogen atom. Given our interest in the use of aldehydes as catalysts, this work was revisited to identify a superior catalyst, o-phthalaldehyde, which facilitates hydrolyses of various organophosphorus compounds bearing P(O)-NH subunits under mild conditions. Interestingly, chemoselective hydrolysis of the P(O)-N bonds could be accomplished in the presence of P(O)-OR bonds.

Substitution of diarylphosphoryl azides with aliphatic amines catalyzed by simple rare-earth metal salts: Efficient and novel preparation of phosphoryl amides

Peng, Xin-Hua,Bai, Rui,Liu, Shanshan,Li, Zhuo,Jiao, Lin-Yu

, (2021/11/05)

A novel and high efficient protocol was disclosed herein for the rare-earth metal salt-catalyzed substitution of phosphoryl azides with amines. In this homogeneous catalysis system, different diarylphosphoryl azides and aliphatic and aromatic amines were

When phosphoryl azide meets mechanochemistry: Clean, rapid, and efficient synthesis of phosphoryl amides under B(C6F5)3catalysis in a ball mill

Jia, Nan,Jiao, Lin-Yu,Li, Zhuo,Peng, Xin-Hua,Wang, Ze-Lin

, p. 6659 - 6665 (2021/10/25)

We described herein the first example associated with B(C6F5)3-catalyzed preparation of phosphoryl amides under mechanochemical conditions. In this novel system, the combination of energetic reagents with an energetic mechanochemical process enabled the r

Transition-metal-free amination phosphoryl azide for the synthesis of phosphoramidates

Li, Qing,Sun, Xiaohua,Yang, Xiaoqin,Wu, Minghu,Sun, Shaofa,Chen, Xiuling

, p. 16040 - 16043 (2019/06/10)

A facile and efficient approach to phosphoramidates was developed via amination of phosphoryl azides. A variety of phosphoramidates were obtained in one step with good to excellent yields under a mild reaction system. The process uses easily available ami

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