Cas 223378-20-9,1-((2R,3R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-3-hydroxy-5-methyl-tetrahydro-furan-2-yl)-5-((E)-2-bromo-vinyl)-1H-pyrimidine-2,4-dione

223378-20-9

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Basic information

Product Name: 1-((2R,3R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-3-hydroxy-5-methyl-tetrahydro-furan-2-yl)-5-((E)-2-bromo-vinyl)-1H-pyrimidine-2,4-dione
Synonyms:
CAS NO:223378-20-9
Molecular Formula:
Molecular Weight: 543.414
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-((2R,3R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-3-hydroxy-5-methyl-tetrahydro-furan-2-yl)-5-((E)-2-bromo-vinyl)-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-((2R,3R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-3-hydroxy-5-methyl-tetrahydro-furan-2-yl)-5-((E)-2-bromo-vinyl)-1H-pyrimidine-2,4-dione(223378-20-9)
EPA Substance Registry System: 1-((2R,3R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-3-hydroxy-5-methyl-tetrahydro-furan-2-yl)-5-((E)-2-bromo-vinyl)-1H-pyrimidine-2,4-dione(223378-20-9)

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: 223378-20-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 223378-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,3,7 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 223378-20:
(8*2)+(7*2)+(6*3)+(5*3)+(4*7)+(3*8)+(2*2)+(1*0)=119
119 % 10 = 9
So 223378-20-9 is a valid CAS Registry Number.

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223378-20-9Relevant academic research and scientific papers

Synthesis of novel 4'-C-methyl-pyrimidine nucleosides and their biological activities

Kitano, Kenji,Machida, Haruhiko,Miura, Shinji,Ohrui, Hiroshi

, p. 827 - 830 (1999)

Two novel 4'-C-methylnucleosides, 4'-methylBVDU 9 and 4'-methylBVaraU 10, were synthesized. The former was derived from 3',5'-di-O-acetyl-2'- deoxy-4'-C-methyluridine 12, and the latter was produced via glycosylation between 4-C-methyl-D-ribose derivative 11 and a silylated bromovinyl uracil. 4'-MethylBVDU 9 exhibited particularly potent anti-varicella-zoster virus (VZV) activity in vitro.

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