Cas 342605-00-9,4-Amino-1-((3R,4R,5S)-3,4-bis-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-2-yl)-1H-pyrimidin-2-one

342605-00-9

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Basic information

Product Name: 4-Amino-1-((3R,4R,5S)-3,4-bis-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-2-yl)-1H-pyrimidin-2-one
Synonyms:
CAS NO:342605-00-9
Molecular Formula:
Molecular Weight: 529.66
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: 4-Amino-1-((3R,4R,5S)-3,4-bis-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-2-yl)-1H-pyrimidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-Amino-1-((3R,4R,5S)-3,4-bis-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-2-yl)-1H-pyrimidin-2-one(342605-00-9)
EPA Substance Registry System: 4-Amino-1-((3R,4R,5S)-3,4-bis-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-2-yl)-1H-pyrimidin-2-one(342605-00-9)

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: 342605-00-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 342605-00-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,6,0 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 342605-00:
(8*3)+(7*4)+(6*2)+(5*6)+(4*0)+(3*5)+(2*0)+(1*0)=109
109 % 10 = 9
So 342605-00-9 is a valid CAS Registry Number.

342605-00-9Upstream product

342604-98-2 1-((3R,4R,5S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-2-yl)-4-[1,2,4]triazol-1-yl-1H-pyrimidin-2-one

342605-00-9Downstream Products

342605-00-9Relevant academic research and scientific papers

Thiosugars. Part 9: Synthesis and biological evaluation of some 4′-thio-L-arabino nucleoside analogues

Wirsching, Joern,Voss, Juergen,Adiwidjaja, Gunadi,Balzarini, Jan,De Clercq, Erik

, p. 1049 - 1051 (2001)

1-O-Acetyl-2, 3, 5-tri-O-benzyl-4-thio-L-arabinofuranose (10) was transformed into the corresponding cytidine derivative 9 and the adenosine derivative 12. Both nucleosides, as well as the previously reported uridine and thymidine analogues 2 and 3, were tested for their in vitro antiviral activity.

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