Cas 87782-40-9,Benzoic acid (2R,3R,4S,5R)-5-[5-((E)-2-bromo-vinyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-4-fluoro-3-hydroxy-tetrahydro-furan-2-ylmethyl ester

87782-40-9

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Basic information

Product Name: Benzoic acid (2R,3R,4S,5R)-5-[5-((E)-2-bromo-vinyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-4-fluoro-3-hydroxy-tetrahydro-furan-2-ylmethyl ester
Synonyms:
CAS NO:87782-40-9
Molecular Formula:
Molecular Weight: 455.237
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: Benzoic acid (2R,3R,4S,5R)-5-[5-((E)-2-bromo-vinyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-4-fluoro-3-hydroxy-tetrahydro-furan-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2R,3R,4S,5R)-5-[5-((E)-2-bromo-vinyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-4-fluoro-3-hydroxy-tetrahydro-furan-2-ylmethyl ester(87782-40-9)
EPA Substance Registry System: Benzoic acid (2R,3R,4S,5R)-5-[5-((E)-2-bromo-vinyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-4-fluoro-3-hydroxy-tetrahydro-furan-2-ylmethyl ester(87782-40-9)

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: 87782-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87782-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,8 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87782-40:
(7*8)+(6*7)+(5*7)+(4*8)+(3*2)+(2*4)+(1*0)=179
179 % 10 = 9
So 87782-40-9 is a valid CAS Registry Number.

87782-40-9Upstream product

87782-40-9Downstream Products

87782-40-9Relevant academic research and scientific papers

Nucleosides. 129. Synthesis of antiviral nucleosides: 5-alkenyl-1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)uracils.

Watanabe,Su,Reichman,Greenberg,Lopez,Fox

, p. 91 - 94 (2007/10/02)

Synthesis of 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)uracils containing a vinyl (4a), 2-halovinyl (4b-d), or ethyl substituent at C-5 was achieved. These nucleosides were found to be about a log order less active than 2'-fluoro-5-iodo-ara-C (FIAC) aga

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