Cas 38183-22-1,1-(6-benzylsulfanyl-purin-9-yl)-O3,O5-hydroxyphosphoryl-β-D-1-deoxy-ribofuranose

38183-22-1

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Basic information

Product Name: 1-(6-benzylsulfanyl-purin-9-yl)-O³,O⁵-hydroxyphosphoryl-β-D-1-deoxy-ribofuranose
Synonyms:
CAS NO:38183-22-1
Molecular Formula:
Molecular Weight: 436.385
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: 1-(6-benzylsulfanyl-purin-9-yl)-O³,O⁵-hydroxyphosphoryl-β-D-1-deoxy-ribofuranose(CAS DataBase Reference)
NIST Chemistry Reference: 1-(6-benzylsulfanyl-purin-9-yl)-O³,O⁵-hydroxyphosphoryl-β-D-1-deoxy-ribofuranose(38183-22-1)
EPA Substance Registry System: 1-(6-benzylsulfanyl-purin-9-yl)-O³,O⁵-hydroxyphosphoryl-β-D-1-deoxy-ribofuranose(38183-22-1)

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: 38183-22-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 38183-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,8 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38183-22:
(7*3)+(6*8)+(5*1)+(4*8)+(3*3)+(2*2)+(1*2)=121
121 % 10 = 1
So 38183-22-1 is a valid CAS Registry Number.

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38183-22-1Relevant academic research and scientific papers

6-Substituted purine 3',5'-cyclic nucleotides

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, (2008/06/13)

Described herein are novel 6-alkylthio and 6-arylalkylthio purine 3',5' cyclic nucleotides variously exhibiting adenyl cyclase and (in animal studies) tumor inhibitory properties, interferon potentiation, antiviral activity, and the ability to activate adenosine 3',5'-cyclic phosphate-dependent protein kinase while enjoying resistance to phosphodiesterase hydrolysis superior to that of its naturally occuring analog. The compounds are obtained by alkylation of the corresponding 6-thio nucleotide, which is in turn provided by a novel synthetic route

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