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Adenosine 5'-[hydrogen [[hydroxy(phosphonooxy)phosphinyl]methyl]phosphonate] is a complex organic compound with the chemical formula C10H15N5O10P2. It is a type of nucleotide, specifically a derivative of adenosine, which is a fundamental component of DNA and RNA. adenosine 5'-[hydrogen [[hydroxy(phosphonooxy)phosphinyl]methyl]phosphonate] features a unique structure where a phosphonate group replaces one of the phosphate groups typically found in natural nucleotides. The presence of the phosphonate group can affect the compound's reactivity and stability, making it a subject of interest in chemical and biological research. It may have potential applications in the development of new drugs or as a tool in molecular biology to study the interactions and functions of nucleotides within cellular processes.

7292-42-4

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7292-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7292-42-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7292-42:
(6*7)+(5*2)+(4*9)+(3*2)+(2*4)+(1*2)=104
104 % 10 = 4
So 7292-42-4 is a valid CAS Registry Number.

7292-42-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-[[hydroxy(phosphonooxy)phosphoryl]methyl]phosphinic acid

1.2 Other means of identification

Product number -
Other names Adenosine 5'-[[hydroxy(phosphonooxy)phosphinyl]methyl] phosphonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7292-42-4 SDS

7292-42-4Downstream Products

7292-42-4Relevant academic research and scientific papers

Combined Phosphoramidite-Phosphodiester Reagents for the Synthesis of Methylene Bisphosphonates

Engelsma, Sander B.,Meeuwenoord, Nico J.,Overkleeft, Hermen S.,van der Marel, Gijsbert A.,Filippov, Dmitri V.

, p. 2955 - 2959 (2017)

A new class of phosphanylmethylphosphonate reagents has been developed to enable the controlled synthesis of methylene bisphosphonate mono- and diesters. Condensation of such reagents with an alcohol of choice through azole-mediated phosphoramidite chemistry followed by in situ oxidation provides orthogonally protected methylene bisphosphonate tetraesters. Global deprotection of the tetraester leads to terminal methylene bisphosphonates. Alternatively, selective deprotection at the terminal phosphonate followed by a condensation between the acquired methylene bisphosphonate triester and a second alcohol leads to methylene bisphosphonates diesters.

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