Cas 162434-75-5,2'-O-(cholest-5-en-3β-yloxycarbonyl)-3'-deoxy-5'-O-(monomethoxytrityl)-N<sup>6</sup>-<2-(4-nitrophenyl)ethoxycarbonyl>adenosine

162434-75-5

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Basic information

Product Name: 2'-O-(cholest-5-en-3β-yloxycarbonyl)-3'-deoxy-5'-O-(monomethoxytrityl)-N⁶-<2-(4-nitrophenyl)ethoxycarbonyl>adenosine
Synonyms: 2'-O-(cholest-5-en-3β-yloxycarbonyl)-3'-deoxy-5'-O-(monomethoxytrityl)-N⁶-<2-(4-nitrophenyl)ethoxycarbonyl>adenosine
CAS NO:162434-75-5
Molecular Formula:
Molecular Weight: 1129.41
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: 2'-O-(cholest-5-en-3β-yloxycarbonyl)-3'-deoxy-5'-O-(monomethoxytrityl)-N⁶-<2-(4-nitrophenyl)ethoxycarbonyl>adenosine(CAS DataBase Reference)
NIST Chemistry Reference: 2'-O-(cholest-5-en-3β-yloxycarbonyl)-3'-deoxy-5'-O-(monomethoxytrityl)-N⁶-<2-(4-nitrophenyl)ethoxycarbonyl>adenosine(162434-75-5)
EPA Substance Registry System: 2'-O-(cholest-5-en-3β-yloxycarbonyl)-3'-deoxy-5'-O-(monomethoxytrityl)-N⁶-<2-(4-nitrophenyl)ethoxycarbonyl>adenosine(162434-75-5)

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: 162434-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 162434-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,4,3 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 162434-75:
(8*1)+(7*6)+(6*2)+(5*4)+(4*3)+(3*4)+(2*7)+(1*5)=125
125 % 10 = 5
So 162434-75-5 is a valid CAS Registry Number.

162434-75-5Upstream product

162434-75-5Downstream Products

162434-76-6 2'-O-(cholest-5-en-3β-yloxycarbonyl)-3'-deoxy-N⁶-<2-(4-nitrophenyl)ethoxycarbonyl>adenosine

162434-75-5Relevant academic research and scientific papers

Nucleotides. Part XLIV. Synthesis, characterization, and biological activity of monomeric and trimeric cordycepin-cholesterol conjugates and inhibition of HIV-1 replication

Wasner,Henderson,Suhadolnik,Pfleiderer

, p. 1757 - 1767 (2007/10/02)

The antivirally active 3'-deoxyadenylyl-(2'-5')-3'-deoxyadenylyl-(2'-5')-3'-deoxyadenosine (cordycepin trimer core) was modified at the 2'- or 5'-terminus, by attachment of cholesterol via a carbonate bond (→15) or a succinate linker (→16 and 27) to impro

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