Cas 87414-30-0,5-(2,5-Dihydroxy-phenyl)-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione

87414-30-0

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Basic information

Product Name: 5-(2,5-Dihydroxy-phenyl)-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione
Synonyms:
CAS NO:87414-30-0
Molecular Formula:
Molecular Weight: 336.301
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-(2,5-Dihydroxy-phenyl)-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2,5-Dihydroxy-phenyl)-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione(87414-30-0)
EPA Substance Registry System: 5-(2,5-Dihydroxy-phenyl)-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione(87414-30-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 87414-30-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87414-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,1 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87414-30:
(7*8)+(6*7)+(5*4)+(4*1)+(3*4)+(2*3)+(1*0)=140
140 % 10 = 0
So 87414-30-0 is a valid CAS Registry Number.

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87414-30-0Relevant academic research and scientific papers

5-p-Benzoquinonyl-2'-deoxyuridine-5'-phosphate: A possible mechanism-based inhibitor of thymidylate synthetase

Maggiora,Chang,Hasson,Bigge,Mertes

, p. 1028 - 1036 (2007/10/02)

The title compound (91), designed as a suicide inhibitor of thymidylate synthetase, can be prepared by silver(II) oxide oxidative demethylation of the corresponding dimethoxyphenyl derivative. Compound 1 shows time-dependent inactivation of thymidylate sy

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