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Dimethylaminophosphonic acid diisopropyl ester, also known as isopropyl methylphosphonofluoridate (IMPF), is an organophosphorus compound with the chemical formula C5H12FNO3P. It is a colorless, oily liquid that is soluble in organic solvents. Dimethylaminophosphonic acid diisopropyl ester is a derivative of dimethylaminophosphonic acid, where two isopropyl groups are attached to the phosphorus atom. It is primarily used as a chemical warfare agent, functioning as a potent inhibitor of the enzyme acetylcholinesterase, which leads to the accumulation of acetylcholine in the nervous system and subsequent disruption of normal nerve function. Due to its high toxicity and potential for misuse, the production and stockpiling of IMPF are strictly regulated under international law.

2404-04-8

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2404-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2404-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2404-04:
(6*2)+(5*4)+(4*0)+(3*4)+(2*0)+(1*4)=48
48 % 10 = 8
So 2404-04-8 is a valid CAS Registry Number.

2404-04-8Downstream Products

2404-04-8Relevant academic research and scientific papers

Dichlorodimethyl hydantoin: An efficient reagent for one-pot synthesis of CWC-related O,O-dialkyl, N,N-dialkyl phosphoramidates

Gupta, Arvind K.,Dubey, Devendra K.,Kaushik

scheme or table, p. 1641 - 1658 (2009/06/18)

A simple, rapid, economical, and efficient one-pot synthetic method for preparation of O,O-dialkyl, N,N-dialkylphosphoramidates (DADAPs) and phosphates has been developed. Copyright Taylor & Francis Group, LLC.

N,N′-dichlorobis(2,4,6-trichlorophenyl)urea (CC-2): An efficient reagent for the synthesis of chemical weapons convention-related dialkyl-N,N-dialkylphosphoramidates from dialkylphosphites

Gupta, Arvind K.,Pardasani, Deepak,Gupta, Hemendra K.,Dubey, Devendra K.

, p. 879 - 882 (2008/09/16)

The present paper describes the one-pot synthesis of dialkyl N,N-dialkylphosphoramidates (DADAP) from dialkylphosphites and dialkylamines using N,N?-dichlorobis(2,4,6-trichlorophenyl)urea (CC-2) as chlorinating reagent. DADAP belong to the schedule 2.B.6 category of the Chemical Weapons Convention (CWC), as they are the important markers of the chemical warfare agent tabun and its analogues. The study was undertaken to develop the spectral database of DADAP for verification of CWC. The reported synthetic strategy can be adopted to rapidly synthesize several analogues of DADAP during official proficiency tests. CSIRO 2007.

ON THE REACTION OF BENZOTHIAZOL-2-YL SULPHENAMIDES WITH PHOSPHITES

Brownbridge, P.,Jowett, I. C.

, p. 311 - 318 (2007/10/02)

A study of the synthesis of phosphoramidates from phosphites and benzothiazol-2-yl-sulphenamides, indicates that a quinquecovalent phosphorane is an intermediate.Since the initial step in this reaction does not involve attack of phosphorus on nitrogen, it is unlikely that these sulphenamides will act as electrophilic aminating agents towards non-phosphorus nucleophiles.An efficient new method for preparing benzothiazol-2-yl-sulphenamides is reported.

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