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diphosphonic acid, P,P-dimethyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32288-17-8

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32288-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32288-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,8 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32288-17:
(7*3)+(6*2)+(5*2)+(4*8)+(3*8)+(2*1)+(1*7)=108
108 % 10 = 8
So 32288-17-8 is a valid CAS Registry Number.

32288-17-8Downstream Products

32288-17-8Relevant academic research and scientific papers

Microwave induced synthesis of O,O-dialkyl dialkylpyrophosphonates under solvent free conditions: Markers of nerve agents

Kumar, Rajesh,Pardasani, Deepak,Mazumder, Avik,Dubey, Devendra K.,Gupta, Arvind K.

, p. 476 - 480 (2008)

This article describes a one pot, solvent free, microwave assisted synthesis of O,O-dialkyl dialkylpyrophosphonates (DADAPP) from O-alkyl alkylphosphonic chlorides 2a?j with 4-dimethylaminopyridine (DMAP) in the presence of water under microwave irradiation. The reaction takes place by the phosphonium salts, which are converted into the DADAPPs 4a?j. These DADAPPs are important markers of chemical warfare agents sarin, soman, and VX and their analogues. The method has several advantages over the conventional methods such as operational simplicity, high yield, and reduced reaction time. CSIRO 2008.

Reaction of VX and GD with gaseous ozone

Wagner, George W.,Bartram, Philip W.,Brickhouse, Mark D.,Connell, Theresa R.,Creasy, William R.,Henderson, Vikki D.,Hovanec, Joseph W.,Morrissey, Kevin M.,Stuff, John R.,Williams, Barry R.

, p. 1267 - 1272 (2007/10/03)

Attempts at decontaminating nerve agents VX {O-ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothioate} and GD (pinacolyl methylphosphonofluoridate) with gaseous ozone are described. VX reacts like a tertiary amine with oxidation occurring at carbons adjacent to the nitrogen. In this manner a variety of novel VX derivatives still possessing intact P-S bonds are generated, and as such, must be considered to retain formidable toxicity. The major product is O-ethyl S-[2-(isopropylamino)ethyl] methylphosphonothioate. No reaction of GD with ozone occurs under the conditions employed.

Phosphorylation of N-trimethylsilyllactams

Uryupin, A. B.,Rakhov, I. A.,Kolesova, V. A.,Petrovskii, P. V.,Mastryukova, T. A.,Kabachnik, M. I.

, p. 1556 - 1560 (2007/10/02)

Treatment of N-trimethylsilyllactams with phosphoryl chlorides results in mixtures of products, whose formation can be explained by competition between N- and O-phosphorylation. - Key words: N-trimethylsilyllactams, dual reactivity; N-phosphoryllactams, synthesis.

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