Cas 477583-38-3,2,4(1H,3H)-Pyrimidinedione, 1-[4-[(acetyloxy)methyl]-3-fluoro-2,5-dihydro-2-furanyl]-5-methyl-

477583-38-3

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Basic information

Product Name: 2,4(1H,3H)-Pyrimidinedione, 1-[4-[(acetyloxy)methyl]-3-fluoro-2,5-dihydro-2-furanyl]-5-methyl-
Synonyms:
CAS NO:477583-38-3
Molecular Formula: C12H13FN2O5
Molecular Weight:
EINECS: N/A
Product Categories: N/A
Mol File: 477583-38-3.mol

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: 2,4(1H,3H)-Pyrimidinedione, 1-[4-[(acetyloxy)methyl]-3-fluoro-2,5-dihydro-2-furanyl]-5-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 1-[4-[(acetyloxy)methyl]-3-fluoro-2,5-dihydro-2-furanyl]-5-methyl-(477583-38-3)
EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 1-[4-[(acetyloxy)methyl]-3-fluoro-2,5-dihydro-2-furanyl]-5-methyl-(477583-38-3)

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: 477583-38-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 477583-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,5,8 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 477583-38:
(8*4)+(7*7)+(6*7)+(5*5)+(4*8)+(3*3)+(2*3)+(1*8)=203
203 % 10 = 3
So 477583-38-3 is a valid CAS Registry Number.

477583-38-3Upstream product

477583-38-3Downstream Products

477583-38-3Relevant academic research and scientific papers

Synthesis of 2',3'-didehydro-2',3'-dideoxy-2'-fluoro apionucleosides as potential antiviral agents

Moon, Hyung Ryong,Kim, Hea Ok,Jeong, Lak Shin

, p. 1800 - 1804 (2002)

Synthesis of novel 2',3'-didehydro-2',3'-dideoxy-2'-fluoro apionucleosides which combine the properties of 2',3'-didehydro-2',3'-dideoxy nucleosides and apionucleosides on the basis of a bioisosteric rationale is described.

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