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Bicyclo[3.1.0]hex-2-ene-6-carbonitrile, 2-methoxy-6-methyl-4-oxo-, (1R,5S,6R)-rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

212609-29-5

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212609-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212609-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,6,0 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 212609-29:
(8*2)+(7*1)+(6*2)+(5*6)+(4*0)+(3*9)+(2*2)+(1*9)=105
105 % 10 = 5
So 212609-29-5 is a valid CAS Registry Number.

212609-29-5Upstream product

212609-29-5Downstream Products

212609-29-5Relevant academic research and scientific papers

Wavelength-Dependent Photochemistry of 4-Methoxybicyclo[3.1.0]hexenones

Dauben, William G.,Hecht, Stefan

, p. 6102 - 6107 (1998)

Wavelength-dependent photochemistry of a series of 4-methoxybicyclo[3.1.0]hexenones is mechanistically investigated. Upon excitation of the symmetry-forbidden S1 n→π* state, photoisomerization is exclusively observed. By comparison of the direct and sensitized quantum yields for this particular process, the T1 π→π* state, which is populated via efficient intersystem crossing as shown by phosphorescence experiments, is proven to be the reactive state. A pathway via external cyclopropane bond cleavage followed by racemization of the formed triplet biradicals reasonably accounts for the observed photostationarity. Excitation of the electric dipole allowed S2 π→π* state initiates phenol formation. The T2 n→π* state, which could not be sensitized, gives a type-B oxyallyl zwitterion via internal cleavage as could be shown by intermolecular as well as intramolecular trapping experiments. The observed data are in good agreement with computational studies.

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