Cas 938062-85-2,1-(2-acetoxyethoxy)methyl-3-methyl-4,6-dibenzylthio-1H-pyrazolo[3,4-d]pyrimidine

938062-85-2

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Basic information

Product Name: 1-(2-acetoxyethoxy)methyl-3-methyl-4,6-dibenzylthio-1H-pyrazolo[3,4-d]pyrimidine
Synonyms: 1-(2-acetoxyethoxy)methyl-3-methyl-4,6-dibenzylthio-1H-pyrazolo[3,4-d]pyrimidine
CAS NO:938062-85-2
Molecular Formula:
Molecular Weight: 494.638
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-(2-acetoxyethoxy)methyl-3-methyl-4,6-dibenzylthio-1H-pyrazolo[3,4-d]pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-acetoxyethoxy)methyl-3-methyl-4,6-dibenzylthio-1H-pyrazolo[3,4-d]pyrimidine(938062-85-2)
EPA Substance Registry System: 1-(2-acetoxyethoxy)methyl-3-methyl-4,6-dibenzylthio-1H-pyrazolo[3,4-d]pyrimidine(938062-85-2)

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: 938062-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 938062-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,8,0,6 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 938062-85:
(8*9)+(7*3)+(6*8)+(5*0)+(4*6)+(3*2)+(2*8)+(1*5)=192
192 % 10 = 2
So 938062-85-2 is a valid CAS Registry Number.

938062-85-2Upstream product

938062-85-2Downstream Products

938062-85-2Relevant academic research and scientific papers

Synthesis and antiviral activity of some C2-, C4-, and C6-substituted pyrazolo[3,4-d]pyrimidine acyclonucleosides with the alkylating chains of ACV, HBG, and iso-DHPG

Moukha-Chafiq, Omar,Taha, Mohamed,Lazrek, Hassan,Vasseur, Jean-Jacques,Clercq, Erik

, p. 849 - 860 (2007/10/03)

A useful route to obtain trisubstituted pyrazolo[3,4-d]pyrimidines 14-17 is described. Those later were coupled with the alkylating agents 18-20 as in ACV, HBG, and iso-DHPG to give, after deprotection, the desired acylonucleosides 33-44 . Almost all of t

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