Cas 778510-92-2,6-N-acetyl-2',3'-O-di-tert-butyldimethylsilyl-7,8-dihydro-8-oxoadenosine 5'-[ethyl N-(N-trityl-L-prolyl)phosphoroamidate]

778510-92-2

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Basic information

Product Name: 6-N-acetyl-2',3'-O-di-tert-butyldimethylsilyl-7,8-dihydro-8-oxoadenosine 5'-[ethyl N-(N-trityl-L-prolyl)phosphoroamidate]
Synonyms: 6-N-acetyl-2',3'-O-di-tert-butyldimethylsilyl-7,8-dihydro-8-oxoadenosine 5'-[ethyl N-(N-trityl-L-prolyl)phosphoroamidate]
CAS NO:778510-92-2
Molecular Formula:
Molecular Weight: 1000.29
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: 6-N-acetyl-2',3'-O-di-tert-butyldimethylsilyl-7,8-dihydro-8-oxoadenosine 5'-[ethyl N-(N-trityl-L-prolyl)phosphoroamidate](CAS DataBase Reference)
NIST Chemistry Reference: 6-N-acetyl-2',3'-O-di-tert-butyldimethylsilyl-7,8-dihydro-8-oxoadenosine 5'-[ethyl N-(N-trityl-L-prolyl)phosphoroamidate](778510-92-2)
EPA Substance Registry System: 6-N-acetyl-2',3'-O-di-tert-butyldimethylsilyl-7,8-dihydro-8-oxoadenosine 5'-[ethyl N-(N-trityl-L-prolyl)phosphoroamidate](778510-92-2)

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: 778510-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 778510-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,8,5,1 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 778510-92:
(8*7)+(7*7)+(6*8)+(5*5)+(4*1)+(3*0)+(2*9)+(1*2)=202
202 % 10 = 2
So 778510-92-2 is a valid CAS Registry Number.

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778510-92-2Relevant academic research and scientific papers

Structure-activity relationship of phosmidosine: Importance of the 7,8-dihydro-8-oxoadenosine residue for antitumor activity

Sekine, Mitsuo,Okada, Kazuhisa,Seio, Kohji,Kakeya, Hideaki,Osada, Hiroyuki,Sasaki, Takuma

, p. 5193 - 5201 (2007/10/03)

To study the structure-activity relationship of phosmidosine, a variety of phosmidosine derivatives 9a-g were synthesized by condensation of N-diisopropyl N′-(N-tritylprolyl)phosphorodiamidite 6 with appropriately protected nucleoside derivatives 7a-g. As

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