Cas 1269050-01-2,(2S,3R,4R,5S)-2-(N<sup>(6)</sup>-benzoyl-adenin-9-yl)-1-(tertbutoxycarbonyl)piperidine-3,4,5-triyl triacetate

1269050-01-2

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Basic information

Product Name: (2S,3R,4R,5S)-2-(N⁽⁶⁾-benzoyl-adenin-9-yl)-1-(tertbutoxycarbonyl)piperidine-3,4,5-triyl triacetate
Synonyms: (2S,3R,4R,5S)-2-(N⁽⁶⁾-benzoyl-adenin-9-yl)-1-(tertbutoxycarbonyl)piperidine-3,4,5-triyl triacetate
CAS NO:1269050-01-2
Molecular Formula:
Molecular Weight: 596.597
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: (2S,3R,4R,5S)-2-(N⁽⁶⁾-benzoyl-adenin-9-yl)-1-(tertbutoxycarbonyl)piperidine-3,4,5-triyl triacetate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R,4R,5S)-2-(N⁽⁶⁾-benzoyl-adenin-9-yl)-1-(tertbutoxycarbonyl)piperidine-3,4,5-triyl triacetate(1269050-01-2)
EPA Substance Registry System: (2S,3R,4R,5S)-2-(N⁽⁶⁾-benzoyl-adenin-9-yl)-1-(tertbutoxycarbonyl)piperidine-3,4,5-triyl triacetate(1269050-01-2)

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: 1269050-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1269050-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,0,5 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1269050-01:
(9*1)+(8*2)+(7*6)+(6*9)+(5*0)+(4*5)+(3*0)+(2*0)+(1*1)=142
142 % 10 = 2
So 1269050-01-2 is a valid CAS Registry Number.

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1269050-01-2Relevant academic research and scientific papers

Synthesis and in vitro anti-hepatitis B virus activity of six-membered azanucleoside analogues

Wang, Dan,Li, Yu-Huan,Wang, Yu-Ping,Gao, Rong-Mei,Zhang, Li-He,Ye, Xin-Shan

experimental part, p. 41 - 51 (2011/02/28)

Fifteen novel six-membered azanucleoside derivatives were prepared and evaluated for their anti-hepatitis B virus (HBV) activity and cytotoxicity in human hepatoblastoma-derived liver Hep-G2 cells. The most potent compound 16b with an IC50 valu

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