Cas 1261065-89-7,5-fluoro-1-[(2S,3S,4S)-4-hydroxy-N-methoxycarbonyl-3-phenylthio-2-pyrrolidinyl]uracil

1261065-89-7

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Basic information

Product Name: 5-fluoro-1-[(2S,3S,4S)-4-hydroxy-N-methoxycarbonyl-3-phenylthio-2-pyrrolidinyl]uracil
Synonyms: 5-fluoro-1-[(2S,3S,4S)-4-hydroxy-N-methoxycarbonyl-3-phenylthio-2-pyrrolidinyl]uracil
CAS NO:1261065-89-7
Molecular Formula:
Molecular Weight: 381.385
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: 5-fluoro-1-[(2S,3S,4S)-4-hydroxy-N-methoxycarbonyl-3-phenylthio-2-pyrrolidinyl]uracil(CAS DataBase Reference)
NIST Chemistry Reference: 5-fluoro-1-[(2S,3S,4S)-4-hydroxy-N-methoxycarbonyl-3-phenylthio-2-pyrrolidinyl]uracil(1261065-89-7)
EPA Substance Registry System: 5-fluoro-1-[(2S,3S,4S)-4-hydroxy-N-methoxycarbonyl-3-phenylthio-2-pyrrolidinyl]uracil(1261065-89-7)

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: 1261065-89-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1261065-89-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,0,6 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1261065-89:
(9*1)+(8*2)+(7*6)+(6*1)+(5*0)+(4*6)+(3*5)+(2*8)+(1*9)=137
137 % 10 = 7
So 1261065-89-7 is a valid CAS Registry Number.

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1261065-89-7Relevant academic research and scientific papers

One-pot conversion of proline derivatives into iodinated iminosugar-based nucleosides, useful precursors of highly functionalized nucleoside analogues

Boto, Alicia,Hernandez, Dacil,Hernandez, Rosendo

, p. 6633 - 6642 (2010)

Readily available proline derivatives can be transformed in one step into β-iodinated iminosugar-based nucleosides, under very mild conditions. The method couples a tandem radical decarboxylation-oxidation-β-iodination to the addition of nitrogen bases. T

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