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Azidomethyl-phosphonic acid diisopropyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17982-56-8

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17982-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17982-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,8 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17982-56:
(7*1)+(6*7)+(5*9)+(4*8)+(3*2)+(2*5)+(1*6)=148
148 % 10 = 8
So 17982-56-8 is a valid CAS Registry Number.

17982-56-8Downstream Products

17982-56-8Relevant academic research and scientific papers

Synthesis and antiproliferative activity of novel α- And β-dialkoxyphosphoryl isothiocyanates

Psurski, Mateusz,Blaewska, Katarzyna,Gajda, Anna,Gajda, Tadeusz,Wietrzyk, Joanna,Oleksyszyn, Jozef

supporting information; experimental part, p. 4572 - 4576 (2011/09/15)

A series of 15 mostly new dialkoxyphosphoryl alkyl and aralkyl isothiocyanates were synthesized using two alternative strategies, and their in vitro antiproliferative activity against several cancer cell lines (including drug resistant) is here demonstrat

Convenient synthesis of dialkyl 1-azidoalkylphosphonates using tetramethylguanidinium azide as azidation agent

Blaszczyk, Roman,Gajda, Tadeusz

, p. 1110 - 1119 (2008/09/18)

A simple and safe method for the preparation of dialkyl 1-azidoalkylphosphonates from dialkyl 1-(4-nitrobenzenesulfonyloxy) alkylphosphonates (dialkyl 1-(nosyloxy)alkylphosphonates) and tetramethylguanidinium azide (TMGA) has been developed. Copyright Tay

A novel synthesis of 1-aminoalkylphosphonates

Chakraborty,Engel

, p. 1039 - 1046 (2007/10/02)

A novel route has been devised for the preparation of a series of 1-aminoalkylphosphonate diesters, precursors to analogues of a-amino acids. The route involves a facile bromine substitution at the 1-position of alkylphosphonate diesters using N-bromosuccinimide, followed by azide ion displacement and catalytic hydrogenolysis.

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