Cas 1198760-89-2,5-methyl-1-[(1S,2R,3S,4R)-2,3,5-tris-benzyloxy-1-benzylsulfanyl-4-hydroxy-pentyl]-1H-pyrimidine-2,4-dione

1198760-89-2

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Basic information

Product Name: 5-methyl-1-[(1S,2R,3S,4R)-2,3,5-tris-benzyloxy-1-benzylsulfanyl-4-hydroxy-pentyl]-1H-pyrimidine-2,4-dione
Synonyms: 5-methyl-1-[(1S,2R,3S,4R)-2,3,5-tris-benzyloxy-1-benzylsulfanyl-4-hydroxy-pentyl]-1H-pyrimidine-2,4-dione
CAS NO:1198760-89-2
Molecular Formula:
Molecular Weight: 652.811
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-methyl-1-[(1S,2R,3S,4R)-2,3,5-tris-benzyloxy-1-benzylsulfanyl-4-hydroxy-pentyl]-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-methyl-1-[(1S,2R,3S,4R)-2,3,5-tris-benzyloxy-1-benzylsulfanyl-4-hydroxy-pentyl]-1H-pyrimidine-2,4-dione(1198760-89-2)
EPA Substance Registry System: 5-methyl-1-[(1S,2R,3S,4R)-2,3,5-tris-benzyloxy-1-benzylsulfanyl-4-hydroxy-pentyl]-1H-pyrimidine-2,4-dione(1198760-89-2)

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: 1198760-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198760-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,7,6 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1198760-89:
(9*1)+(8*1)+(7*9)+(6*8)+(5*7)+(4*6)+(3*0)+(2*8)+(1*9)=212
212 % 10 = 2
So 1198760-89-2 is a valid CAS Registry Number.

1198760-89-2Upstream product

1198760-89-2Downstream Products

1198761-00-0 (1R,2R,3R,4S)-methanesulfonic acid 2,3-bis-benzyloxy-1-benzyloxymethyl-4-benzylsulfanyl-4-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-butyl ester

1198760-89-2Relevant academic research and scientific papers

A stereoselective approach to nucleosides and 4′-thioanalogues from acyclic precursors

Chapdelaine, Daniel,Cardinal-David, Benoit,Prevost, Michel,Gagnon, Marc,Thumin, Isabelle,Guindon, Yvan

supporting information; experimental part, p. 17242 - 17245 (2010/03/25)

D- and L-nucleosides and analogues thereof, including the 4′-thionucleoside series, are one of the most important biological and pharmaceutically active classes of compounds. A novel approach to their synthesis from chiral acyclic thioaminal, bearing the nucleobase, is described.

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