Cas 913832-70-9,(5R,8S,10S,11R)-10,11-bis(acetyloxy)-5,8-dihydro-2-phenyl-5,8-etheno-1H-[1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione

913832-70-9

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Basic information

Product Name: (5R,8S,10S,11R)-10,11-bis(acetyloxy)-5,8-dihydro-2-phenyl-5,8-etheno-1H-[1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione
Synonyms: (5R,8S,10S,11R)-10,11-bis(acetyloxy)-5,8-dihydro-2-phenyl-5,8-etheno-1H-[1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione
CAS NO:913832-70-9
Molecular Formula:
Molecular Weight: 371.349
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: (5R,8S,10S,11R)-10,11-bis(acetyloxy)-5,8-dihydro-2-phenyl-5,8-etheno-1H-[1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: (5R,8S,10S,11R)-10,11-bis(acetyloxy)-5,8-dihydro-2-phenyl-5,8-etheno-1H-[1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione(913832-70-9)
EPA Substance Registry System: (5R,8S,10S,11R)-10,11-bis(acetyloxy)-5,8-dihydro-2-phenyl-5,8-etheno-1H-[1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione(913832-70-9)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 913832-70-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 913832-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,8,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 913832-70:
(8*9)+(7*1)+(6*3)+(5*8)+(4*3)+(3*2)+(2*7)+(1*0)=169
169 % 10 = 9
So 913832-70-9 is a valid CAS Registry Number.

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913832-70-9Relevant academic research and scientific papers

Cis-3,5-cyclohexadiene-1,2-diol derivatives: Facial selectivity in their Diels-Alder reactions with ethylenic, acetylenic and azo dienophiles

Ogbomo, Sunny M.,Burnell, D. Jean

, p. 3838 - 3848 (2008/09/18)

The Diels-Alder reactions of maleimide with the acetonide derivative (6a) of cis-3,5-cyclohexadiene-1,2-diol (1a) in various solvents showed facial selectivities ranging from 1: 1 to 1: 9. The same derivative 6a reacted in benzene with ethylenic dienophil

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