Cas 99790-16-6,7,8-dihydro-2',3'-O-isopropylidene-7-phenoxycarbonyl-N<sup>6</sup>-propylcarbamoyl-8,5'-O-cycloadenosine

99790-16-6

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Basic information

Product Name: 7,8-dihydro-2',3'-O-isopropylidene-7-phenoxycarbonyl-N⁶-propylcarbamoyl-8,5'-O-cycloadenosine
Synonyms:
CAS NO:99790-16-6
Molecular Formula:
Molecular Weight: 512.522
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: 7,8-dihydro-2',3'-O-isopropylidene-7-phenoxycarbonyl-N⁶-propylcarbamoyl-8,5'-O-cycloadenosine(CAS DataBase Reference)
NIST Chemistry Reference: 7,8-dihydro-2',3'-O-isopropylidene-7-phenoxycarbonyl-N⁶-propylcarbamoyl-8,5'-O-cycloadenosine(99790-16-6)
EPA Substance Registry System: 7,8-dihydro-2',3'-O-isopropylidene-7-phenoxycarbonyl-N⁶-propylcarbamoyl-8,5'-O-cycloadenosine(99790-16-6)

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: 99790-16-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 99790-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,7,9 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99790-16:
(7*9)+(6*9)+(5*7)+(4*9)+(3*0)+(2*1)+(1*6)=196
196 % 10 = 6
So 99790-16-6 is a valid CAS Registry Number.

99790-16-6Upstream product

99790-16-6Downstream Products

99790-16-6Relevant academic research and scientific papers

Mechanism of the Phenoxycarbonylation of 2',3'-O-Isopropylidenadenosine

Anzai, Kentaro,Uzawa, Jun

, p. 1309 - 1315 (2007/10/02)

1H-NMR-spektroskopische Verfolgung des zeitlichen Ablaufs der Umsetzung von 2',3'-O-Isopropylidenadenosin (1) mit Chlorameisensaeure-phenylester ergibt, dass zunaechst Reaktion an N7 von 1 zum Cyclonucleosid 12 erfolgt, letzteres lagert sich langsam in die 5'-O-Phenoxycarbonyl-Verbindung 3 um.Die Reaktionen des dreifach triphenoxycarbonylierten Cycloadenosins 11 mit Aminen und Alkoholen werden ebenfalls beschrieben.

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