Cas 163586-75-2,Acetic acid (2R,3S,5R)-5-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-(2-thioxo-2λ<sup>5</sup>-[1,3,2]dithiaphospholan-2-yloxymethyl)-tetrahydro-furan-3-yl ester

163586-75-2

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Basic information

Product Name: Acetic acid (2R,3S,5R)-5-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-(2-thioxo-2λ⁵-[1,3,2]dithiaphospholan-2-yloxymethyl)-tetrahydro-furan-3-yl ester
Synonyms:
CAS NO:163586-75-2
Molecular Formula:
Molecular Weight: 527.583
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: Acetic acid (2R,3S,5R)-5-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-(2-thioxo-2λ⁵-[1,3,2]dithiaphospholan-2-yloxymethyl)-tetrahydro-furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3S,5R)-5-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-(2-thioxo-2λ⁵-[1,3,2]dithiaphospholan-2-yloxymethyl)-tetrahydro-furan-3-yl ester(163586-75-2)
EPA Substance Registry System: Acetic acid (2R,3S,5R)-5-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-(2-thioxo-2λ⁵-[1,3,2]dithiaphospholan-2-yloxymethyl)-tetrahydro-furan-3-yl ester(163586-75-2)

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: 163586-75-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 163586-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,5,8 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 163586-75:
(8*1)+(7*6)+(6*3)+(5*5)+(4*8)+(3*6)+(2*7)+(1*5)=162
162 % 10 = 2
So 163586-75-2 is a valid CAS Registry Number.

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163586-75-2Relevant academic research and scientific papers

The synthesis of nucleoside 5'-O-(1,1-dithiotriphosphates)

Okruszek,Olesiak,Balzarini

, p. 3850 - 3854 (2007/10/02)

Appropriately protected nucleoside 5'-O-(2-thio-1,3,2-dithiaphospholanes) react with inorganic pyrophosphate in the presence of a strong base catalyst (DBU) to give nucleoside 5'-O-(1,1-dithiotriphosphates) 1a-g. The latter compounds, including an AZT analogue, show modest antivirial activity against HIV-1 and HIV-2 replication in CEM cells. The AZT and deoxyadenosine derivatives were found to be inhibitors of HIV reverse transcriptase.

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