Cas 925683-49-4,{1-[4-(2-methoxy-ethylamino)-2-oxo-2<i>H</i>-pyrimidin-1-ylmethyl]-2-trityloxy-ethoxymethyl}-phosphonic acid diisopropyl ester

925683-49-4

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Basic information

Product Name: {1-[4-(2-methoxy-ethylamino)-2-oxo-2H-pyrimidin-1-ylmethyl]-2-trityloxy-ethoxymethyl}-phosphonic acid diisopropyl ester
Synonyms:
CAS NO:925683-49-4
Molecular Formula:
Molecular Weight: 663.751
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: {1-[4-(2-methoxy-ethylamino)-2-oxo-2H-pyrimidin-1-ylmethyl]-2-trityloxy-ethoxymethyl}-phosphonic acid diisopropyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {1-[4-(2-methoxy-ethylamino)-2-oxo-2H-pyrimidin-1-ylmethyl]-2-trityloxy-ethoxymethyl}-phosphonic acid diisopropyl ester(925683-49-4)
EPA Substance Registry System: {1-[4-(2-methoxy-ethylamino)-2-oxo-2H-pyrimidin-1-ylmethyl]-2-trityloxy-ethoxymethyl}-phosphonic acid diisopropyl ester(925683-49-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 925683-49-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 925683-49-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,6,8 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 925683-49:
(8*9)+(7*2)+(6*5)+(5*6)+(4*8)+(3*3)+(2*4)+(1*9)=204
204 % 10 = 4
So 925683-49-4 is a valid CAS Registry Number.

925683-49-4Upstream product

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925683-49-4Relevant academic research and scientific papers

Synthesis of some N4-substituted derivatives of 1-[(S)-3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (HPMPC, cidofovir)

Chalupova, Sarka,Holy, Antonin,Masojidkova, Milena

, p. 2053 - 2065 (2007/10/03)

N4-Substituted derivatives of HPMPC were synthesized in four-step synthesis which included treatment of 4-methoxypyrimidin-2(1H)-one (1) with (S)-[(trityloxy)methyl]oxirane in DMF. Condensation of intermediary 1-[2-hydroxy-3-(trityloxy)propyl]-

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