Cas 1334715-84-2,5-decyloxymethyl-1-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione

1334715-84-2

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Basic information

Product Name: 5-decyloxymethyl-1-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione
Synonyms: 5-decyloxymethyl-1-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione
CAS NO:1334715-84-2
Molecular Formula:
Molecular Weight: 726.824
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-decyloxymethyl-1-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-decyloxymethyl-1-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione(1334715-84-2)
EPA Substance Registry System: 5-decyloxymethyl-1-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione(1334715-84-2)

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: 1334715-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1334715-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,7,1 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1334715-84:
(9*1)+(8*3)+(7*3)+(6*4)+(5*7)+(4*1)+(3*5)+(2*8)+(1*4)=152
152 % 10 = 2
So 1334715-84-2 is a valid CAS Registry Number.

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1334715-84-2Relevant academic research and scientific papers

Synthesis of various 5-alkoxymethyluracil analogues and structure-cytotoxic activity relationship study

Brulíková, Lucie,D?ubák, Petr,Hajdúch, Marián,Hlavá?, Jan

, p. 2136 - 2144 (2011/11/06)

A number of 5-alkoxymethyluracil analogues were synthesized to evaluate their cytotoxic activity. 5-Alkoxymethyluracil derivatives 1 were prepared via known nucleophilic substitution of 5-chloromethyluracil 5 and subsequently transformed to their correspo

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