Cas 148440-99-7,2,4-dimethoxy-(2'S)-trans-5-<2',5'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine

148440-99-7

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Basic information

Product Name: 2,4-dimethoxy-(2'S)-trans-5-<2',5'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine
Synonyms: 2,4-dimethoxy-(2'S)-trans-5-<2',5'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine
CAS NO:148440-99-7
Molecular Formula:
Molecular Weight: 480.563
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: 2,4-dimethoxy-(2'S)-trans-5-<2',5'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 2,4-dimethoxy-(2'S)-trans-5-<2',5'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine(148440-99-7)
EPA Substance Registry System: 2,4-dimethoxy-(2'S)-trans-5-<2',5'-dihydro-5'-<(triphenylmethoxy)methyl>-2'-furanyl>pyrimidine(148440-99-7)

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: 148440-99-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 148440-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,4,4 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 148440-99:
(8*1)+(7*4)+(6*8)+(5*4)+(4*4)+(3*0)+(2*9)+(1*9)=147
147 % 10 = 7
So 148440-99-7 is a valid CAS Registry Number.

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148440-99-7Relevant academic research and scientific papers

Enantio- and Diastereoisomers of 2,4-Dimethoxy-5-(2,3-dideoxy-5-O-tritylribofuranosyl)pyrimidine. 2',3'-Dideoxy Pyrimidine C-Nucleosides by Palladium-Mediated Glycal-Aglycon Coupling

Zhang, Han-Cheng,Daves, G. Doyle

, p. 2557 - 2560 (2007/10/02)

Newly available enantiomeric 2,3-dideoxy glycals, (5S)- and (5R)-4,5-dihydro-5-furans and 2,4-dimethoxy-5-iodopyrimidine undergo palladium-mediated coupling by two different, complementary procedures to form enantiomeric pairs of

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