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Diethyl benzyl(phenyl)phosphoramidate is a complex organic compound with the chemical formula C21H24NO2P. It is a colorless to pale yellow liquid with a molecular weight of 353.39 g/mol. diethyl benzyl(phenyl)phosphoramidate is characterized by its phosphorus-nitrogen bond and is derived from the combination of diethyl phosphite, benzyl chloride, and phenyl isocyanate. It is used as a precursor in the synthesis of various agrochemicals, particularly as a building block for the production of pesticides. Due to its reactivity and potential toxicity, it is important to handle this chemical with care, following appropriate safety protocols.

7006-55-5

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7006-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7006-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7006-55:
(6*7)+(5*0)+(4*0)+(3*6)+(2*5)+(1*5)=75
75 % 10 = 5
So 7006-55-5 is a valid CAS Registry Number.

7006-55-5Downstream Products

7006-55-5Relevant academic research and scientific papers

Harnessing Thin-Film Continuous-Flow Assembly Lines

Britton, Joshua,Castle, Jared W.,Weiss, Gregory A.,Raston, Colin L.

, p. 10773 - 10776 (2016)

Inspired by nature's ability to construct complex molecules through sequential synthetic transformations, an assembly line synthesis of α-aminophosphonates has been developed. In this approach, simple starting materials are continuously fed through a thin-film reactor where the intermediates accrue molecular complexity as they progress through the flow system. Flow chemistry allows rapid multistep transformations to occur via reaction compartmentalization, an approach not amenable to using conventional flasks. Thin film processing can also access facile in situ solvent exchange to drive reaction efficiency, and through this method, α-aminophosphonate synthesis requires only 443 s residence time to produce 3.22 g h?1. Assembly-line synthesis allows unprecedented reaction flexibility and processing efficiency.

Copper-Phosphine Mediated Oxidative Phosphorylation of Aromatic Amines and P(OR)3 under Aerobic Conditions

Wang, Shihaozhi,Ma, Shidi,Yang, Jiale,Li, Wenshuang,Li, Dianjun,Yang, Jinhui

supporting information, p. 4278 - 4283 (2021/06/16)

A copper-phosphine system (Cu(OAc)2 and t-Bu3P?HBF4) was used to synthesize α-aminophosphonates and phosphoramides from various aromatic amines and trialkyl phosphites under oxygen atmosphere. With this Cu?P system, α-aminophosphonates containing C?P bonds were generated from N,N-dimethylanilines or N-methylanilines and trialkyl phosphites; phosphoramidates containing N?P bonds were produced from N-benzylanilines and trialkyl phosphites. This strategy provided a convenient and efficient method for the synthesis of phosphorous compounds. The compounds containing phosphoryl group attracted extensive attention due to their biological activities and wide applications.[1,2] The α-aminophosphonates have been applied in medicine and agriculture such as anticancer drugs, antibiotics, antibacterial agents, and enzyme inhibitors.[1] And phosphoramides could be served as antibiotics, prodrugs, flame retardants, and ligands.[2].

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