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3,6-Methanobenzofuran-2(3H)-one, hexahydro- is a chemical compound with the molecular formula C7H10O2. It is a heterocyclic organic compound, specifically a benzofuran derivative, which features a benzene ring fused to a furan ring with an additional methylene bridge. The compound is characterized by the presence of a lactone group, which is a cyclic ester, in this case, a 2(3H)-one group. This structure contributes to its reactivity and potential applications in various chemical processes. The hexahydro prefix indicates that the compound has six hydrogen atoms in a cyclic structure, which can influence its physical and chemical properties. 3,6-Methanobenzofuran-2(3H)-one, hexahydro- may be of interest in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and reactivity.

6715-18-0

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6715-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6715-18-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6715-18:
(6*6)+(5*7)+(4*1)+(3*5)+(2*1)+(1*8)=100
100 % 10 = 0
So 6715-18-0 is a valid CAS Registry Number.

6715-18-0Upstream product

6715-18-0Relevant academic research and scientific papers

222. Inductivity and Bridging in 2-Bicyclooctyl Cations. Polar Effects, Part II.

Grob, Cyril A.,Sawlewicz, Pawel

, p. 1906 - 1917 (2007/10/02)

The solvolysis rates and products of several 6-substituted 2-exo- and 2-endo-bicyclooctyl p-toluenesulfonates, 12 and 13, respectively, are reported.Inductivity, as measured by the reaction constants pI, is considerably less in the exo-series 12 (pI = -1.50) than in the corresponding 2-exo-norbornyl p-toluenesulfonates 1 (pI = -2.0).It is proposed that, for geometrical reasons, bridging of the cationic center C(2) by C(6) is not as strong in the bicyclooctane series 12 as it is in the norbornane series 1.On the other hand, inductivity is higher in the 2-endo-bicyclooctane series 13 (pI = -1.0) than in the corresponding 2-endo-norbornane series 3 (pI = 0.78), probably, because in the former case bridging of C(6) is less hindered by the departing anion.The relative yields of exo- and endo-substitution products from the series 12 and 13, are in accord with graded bridging of C(6) in the incipient bicyclooctyl cations.But almost constant bridging of C(2) by C(7) is indicated in the ionization of the 2-endo-bicyclooctane series 13.Consequently, in the free unsubstituted bicyclooctane cation C(2) is bridged symmetrically by C(6) and C(7), in contrast to the current concept of 'non-classical' two-electron-three-center bonding.

216. Bicyclooctanes. Syntheses and Hydrolyses of 6-exo-substituted 2-exo- and 2-endo-Bicyclooctyl p-Toluenesulfonates. Part 9

Grob, Cyril A.,Sawlewicz, Pawel

, p. 1859 - 1867 (2007/10/02)

The synthesis of the title compounds and their hydrolysis products in 70percent dioxane are described.

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