Cas 1258599-06-2,2-((2R,3S,4R,5R)-5-(2,4-dioxo-6-phenyl-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)ethylphosphonic acid

1258599-06-2

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Basic information

Product Name: 2-((2R,3S,4R,5R)-5-(2,4-dioxo-6-phenyl-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)ethylphosphonic acid
Synonyms:
CAS NO:1258599-06-2
Molecular Formula:
Molecular Weight: 398.309
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: 2-((2R,3S,4R,5R)-5-(2,4-dioxo-6-phenyl-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)ethylphosphonic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-((2R,3S,4R,5R)-5-(2,4-dioxo-6-phenyl-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)ethylphosphonic acid(1258599-06-2)
EPA Substance Registry System: 2-((2R,3S,4R,5R)-5-(2,4-dioxo-6-phenyl-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)ethylphosphonic acid(1258599-06-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1258599-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1258599-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,5,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1258599-06:
(9*1)+(8*2)+(7*5)+(6*8)+(5*5)+(4*9)+(3*9)+(2*0)+(1*6)=202
202 % 10 = 2
So 1258599-06-2 is a valid CAS Registry Number.

1258599-06-2Upstream product

1258599-04-0 C₁₉H₂₃N₂O₈P

1258599-06-2Downstream Products

1258599-06-2Relevant academic research and scientific papers

Synthesis of C-6-substituted uridine phosphonates through aerobic ligand-free Suzuki-Miyaura cross-coupling

Nencka, Radim,Sinnaeve, Davy,Karalic, Izet,Martins, Jose C.,Van Calenbergh, Serge

experimental part, p. 5234 - 5246 (2010/12/25)

An efficient protocol for the construction of C-6-(hetero)aryl-substituted uridine phosphonate analogues utilizing an aerobic, ligand-free Suzuki-Miyaura cross-coupling reaction of a 6-iodo-precursor in aqueous media has been established. The method presents a modular approach toward the target compounds as demonstrated by the synthesis of a small library comprising 14 novel nucleoside phosphonates.

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