Cas 1385029-92-4,6-ethyl-3-{[3-(naphthalen-1-yl)-1,2,4-oxadiazol-5-yl]methyl}-5-phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7(6H)-one

1385029-92-4

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Product Name: 6-ethyl-3-{[3-(naphthalen-1-yl)-1,2,4-oxadiazol-5-yl]methyl}-5-phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7(6H)-one
Synonyms: 6-ethyl-3-{[3-(naphthalen-1-yl)-1,2,4-oxadiazol-5-yl]methyl}-5-phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7(6H)-one
CAS NO:1385029-92-4
Molecular Formula:
Molecular Weight: 449.472
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-ethyl-3-{[3-(naphthalen-1-yl)-1,2,4-oxadiazol-5-yl]methyl}-5-phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7(6H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 6-ethyl-3-{[3-(naphthalen-1-yl)-1,2,4-oxadiazol-5-yl]methyl}-5-phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7(6H)-one(1385029-92-4)
EPA Substance Registry System: 6-ethyl-3-{[3-(naphthalen-1-yl)-1,2,4-oxadiazol-5-yl]methyl}-5-phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7(6H)-one(1385029-92-4)

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: 1385029-92-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1385029-92-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,5,0,2 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1385029-92:
(9*1)+(8*3)+(7*8)+(6*5)+(5*0)+(4*2)+(3*9)+(2*9)+(1*2)=174
174 % 10 = 4
So 1385029-92-4 is a valid CAS Registry Number.

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1385029-92-4Relevant academic research and scientific papers

Synthesis and antimicrobial activity of new 1,2,3-triazolopyrimidine derivatives and their glycoside and acyclic nucleoside analogs

El-Sayed, Wael A.,Ali, Omar M.,Faheem, Merfat S.,Zied, Ibrahim F.,Abdel-Rahman, Adel A.-H.

, p. 607 - 612 (2012/09/07)

New [1,2,4-oxadiazolyl]methyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin derivatives were synthesized starting from N'-Hydroxy-1-naphthimidamide. The N-substituted acyclic nucleoside analogs as well as the substituted glycosides were also prepared by reaction wit

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