Cas 897931-72-5,N<sup>4</sup>-benzoyl-1-{(S)-2-[(diisopropoxyphosphoryl)methoxy]-3-(triphenylmethoxy)propyl}-5-iodocytosine

897931-72-5

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Basic information

Product Name: N⁴-benzoyl-1-{(S)-2-[(diisopropoxyphosphoryl)methoxy]-3-(triphenylmethoxy)propyl}-5-iodocytosine
Synonyms: N⁴-benzoyl-1-{(S)-2-[(diisopropoxyphosphoryl)methoxy]-3-(triphenylmethoxy)propyl}-5-iodocytosine
CAS NO:897931-72-5
Molecular Formula:
Molecular Weight: 835.676
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: N⁴-benzoyl-1-{(S)-2-[(diisopropoxyphosphoryl)methoxy]-3-(triphenylmethoxy)propyl}-5-iodocytosine(CAS DataBase Reference)
NIST Chemistry Reference: N⁴-benzoyl-1-{(S)-2-[(diisopropoxyphosphoryl)methoxy]-3-(triphenylmethoxy)propyl}-5-iodocytosine(897931-72-5)
EPA Substance Registry System: N⁴-benzoyl-1-{(S)-2-[(diisopropoxyphosphoryl)methoxy]-3-(triphenylmethoxy)propyl}-5-iodocytosine(897931-72-5)

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: 897931-72-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 897931-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,9,3 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 897931-72:
(8*8)+(7*9)+(6*7)+(5*9)+(4*3)+(3*1)+(2*7)+(1*2)=245
245 % 10 = 5
So 897931-72-5 is a valid CAS Registry Number.

897931-72-5Upstream product

148873-52-3 bis(2-propyl) N⁴-benzoyl-1-(S)-(2-phosphonomethoxy-3-triphenylmethoxypropyl)cytosine

897931-72-5Downstream Products

897931-72-5Relevant academic research and scientific papers

Preparation of C-5 substituted cidofovir derivatives

Krecmerova, Marcela,Masojidkova, Milena,Holy, Antonin

, p. 579 - 594 (2006)

1-[(S)-3-Hydroxy-2-(phosphonomethoxy)propyl]cytosine (HPMPC, cidofovir) was modified by substitution on the base moiety in positions C-S and N4. Key intermediates of these syntheses, diisopropyl esters of (S)-1-[2-(phosphonomethoxy)-3-(tripheny

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