Cas 155446-91-6,2-((2R,3S,5R)-3-Fluoro-5-phenylsulfanyl-tetrahydro-furan-2-ylmethoxy)-4-methoxy-5-methyl-pyrimidine

155446-91-6

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Basic information

Product Name: 2-((2R,3S,5R)-3-Fluoro-5-phenylsulfanyl-tetrahydro-furan-2-ylmethoxy)-4-methoxy-5-methyl-pyrimidine
Synonyms: 2-((2R,3S,5R)-3-Fluoro-5-phenylsulfanyl-tetrahydro-furan-2-ylmethoxy)-4-methoxy-5-methyl-pyrimidine
CAS NO:155446-91-6
Molecular Formula:
Molecular Weight: 350.414
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-((2R,3S,5R)-3-Fluoro-5-phenylsulfanyl-tetrahydro-furan-2-ylmethoxy)-4-methoxy-5-methyl-pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 2-((2R,3S,5R)-3-Fluoro-5-phenylsulfanyl-tetrahydro-furan-2-ylmethoxy)-4-methoxy-5-methyl-pyrimidine(155446-91-6)
EPA Substance Registry System: 2-((2R,3S,5R)-3-Fluoro-5-phenylsulfanyl-tetrahydro-furan-2-ylmethoxy)-4-methoxy-5-methyl-pyrimidine(155446-91-6)

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: 155446-91-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155446-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,4,4 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155446-91:
(8*1)+(7*5)+(6*5)+(5*4)+(4*4)+(3*6)+(2*9)+(1*1)=146
146 % 10 = 6
So 155446-91-6 is a valid CAS Registry Number.

155446-91-6Upstream product

135292-35-2 2‐chloro‐4‐methoxy‐5‐methylpyrimidine

155446-91-6Downstream Products

25526-93-6 alovudine

155446-91-6Relevant academic research and scientific papers

Stereocontrolled synthesis of pyrimidine 2',3'-dideoxy-β-nucleosides by intramolecular glycosylation

Sujino,Sugimura

, p. 1883 - 1886 (1994)

β-2',3'-Dideoxynucleosides and their 3'-azido and 3'-fluoro substituted derivatives were synthesized in a stereocontrolled manner by the dimethyl(methylthio)sulfonium tetrafluoroborate promoted intramolecular glycosylation of phenyl 2,3-dideoxy-5-O-(2-pyrimidyl)-1-thioglycosides followed by hydrolysis or ammonolysis.

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