Cas 191281-81-9,1-hydroperoxy-1-(1-methylethenyl)-4-(4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl)-pentane

191281-81-9

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Basic information

Product Name: 1-hydroperoxy-1-(1-methylethenyl)-4-(4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl)-pentane
Synonyms:
CAS NO:191281-81-9
Molecular Formula:
Molecular Weight: 268.353
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-hydroperoxy-1-(1-methylethenyl)-4-(4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl)-pentane(CAS DataBase Reference)
NIST Chemistry Reference: 1-hydroperoxy-1-(1-methylethenyl)-4-(4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl)-pentane(191281-81-9)
EPA Substance Registry System: 1-hydroperoxy-1-(1-methylethenyl)-4-(4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl)-pentane(191281-81-9)

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: 191281-81-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 191281-81-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,2,8 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 191281-81:
(8*1)+(7*9)+(6*1)+(5*2)+(4*8)+(3*1)+(2*8)+(1*1)=139
139 % 10 = 9
So 191281-81-9 is a valid CAS Registry Number.

191281-81-9Upstream product

191281-81-9Downstream Products

191281-81-9Relevant academic research and scientific papers

Antimalarial activity of 1,4-epidioxy-bisabola-2,12-diene derivatives

Ruecker, Gerhard,Breitmaier, Eberhard,Manns, Detlef,Maier, Walter,Marek, Anne,Heinzmann, Berta,Heiden, Klemens,Seggewies, Stephan

, p. 12 - 16 (1997)

1,4-Epidoxy-bisabola-2,12-dien (3) and aromatic hydroperoxides (4, 5) were prepared by photoxidation of γ-curcumene (1). Reduction and esterification of 6 and 7 afforded compounds 9 to 10. All compounds were tested in vitro for antimalarial activity. The activity could not be increased significantly, compared with 3. The most active compounds, 3 and 9, did not show in vivo antimalarial activity in mice.

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