Cas 127589-13-3,1-((1R,3S,4R)-3-Fluoro-4-trityloxymethyl-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione

127589-13-3

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Basic information

Product Name: 1-((1R,3S,4R)-3-Fluoro-4-trityloxymethyl-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione
Synonyms:
CAS NO:127589-13-3
Molecular Formula:
Molecular Weight: 484.57
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-((1R,3S,4R)-3-Fluoro-4-trityloxymethyl-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-((1R,3S,4R)-3-Fluoro-4-trityloxymethyl-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione(127589-13-3)
EPA Substance Registry System: 1-((1R,3S,4R)-3-Fluoro-4-trityloxymethyl-cyclopentyl)-5-methyl-1H-pyrimidine-2,4-dione(127589-13-3)

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: 127589-13-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127589-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,8 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127589-13:
(8*1)+(7*2)+(6*7)+(5*5)+(4*8)+(3*9)+(2*1)+(1*3)=153
153 % 10 = 3
So 127589-13-3 is a valid CAS Registry Number.

127589-13-3Upstream product

125353-61-9 carbocyclic 5'-O-trityl-3'-epi-thymidine

127589-13-3Downstream Products

127589-13-3Relevant academic research and scientific papers

SYNTHETIC STUDIES TOWARDS (-)-CARBA-3'-DEOXY-3'-FLUOROTHYMIDINE

Beres, J.,Sagi, Gy.,Baitz-Gacs, E.,Toemoeskoezi, I.,Gruber, L.,Oetvoes, L.

, p. 6271 - 6280 (1989)

Stereospecific synthesis of (-)-carba-3'-deoxy-3'-fluorothymidine (-)-11 is reported from the protected (-)-carbocyclic 3'-epi-thymidine (-)-7 using diethylaminosulfur trifluoride.Under the conditions used, extensive dehydration of the blocked precursor i

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