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1,2-Dimethyltricyclo[3.3.0.02,7]octan-3-one is a complex organic compound with the molecular formula C11H18O. It is a cyclic ketone, characterized by the presence of a carbonyl group (C=O) and a three-ring structure. The compound features two methyl groups (CH3) attached to the carbon atoms at positions 1 and 2 of the tricyclic ring system. This molecule is known for its unique structure and potential applications in various chemical and pharmaceutical industries. Due to its complex structure, it may exhibit specific chemical properties and reactivity, making it a subject of interest for researchers in organic chemistry.

465-36-1

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465-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 465-36-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 465-36:
(5*4)+(4*6)+(3*5)+(2*3)+(1*6)=71
71 % 10 = 1
So 465-36-1 is a valid CAS Registry Number.

465-36-1Downstream Products

465-36-1Relevant academic research and scientific papers

Sensory Importance and Mechanism of Photochemical Conversion of Carvone to Carvonecamphor in Ethanol-Water Mixtures

Refsgaard, Hanne H. F.,Nielsen, Bo R.,Skibsted, Leif H.

, p. 1177 - 1183 (2007/10/02)

Approximate odor thresholds for carvonecamphor, with camphor odor, and for the ester hexyl>acetate>, with sweet odor, were determined to be 2200-4100 and 1.8-2.5 ppb, respectively, by gas chromatographic effluent sniffing.The quantum yield of photochemical conversion of carvone to carvonecamphor showed no wavelength dependence but increased with decreasing ethanol content in ethanol-water mixtures: 0.049 +/- 0.008 mol*eistein-1 in 42percent ethanol (apparent activation energy of 19 kJ*mol-1) and 0.0033 +/- 0.00015 mol*einstein-1 in neat ethanol.The quantum yield of further conversion of carvonecamphor to the ester was approximately 0.1 mol*einstein-1.The triplet lifetime of carvone determined by laser flash spectroscopy in the absence of oxygen increased with decreasing ethanol content: 71 ns in neat, 76 ns in 80percent, and 98 ns in 42percent ethanol.Oxygen quenched the triplet excited state with kO2 ca.3*109 L*mol-1*s-1 whereas oxygen, piperylene, and diacetyl did not influence the photochemical conversion.Intramolecular electron transfer from an n?* singlet state of carvone is suggested to be responsible for the photocycloaddition reaction of carvone.Keywords: (+)-Carvone; carvonecamphor; ethyl 2-hexyl>acetate; odor thresholds; gas chromatography-olfactometry; photocycloaddition

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