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Octahydro-1,2,4-methenopentalene is a cyclic hydrocarbon compound with the molecular formula C7H12. It is a colorless liquid with a pungent odor and is derived from the hydrogenation of 1,2,4-trimethylbenzene. Octahydro-1,2,4-methenopentalene is characterized by its unique structure, which consists of a seven-membered ring with alternating single and double bonds, and a methyl group attached to one of the carbon atoms. Octahydro-1,2,4-methenopentalene is an important intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its chemical reactivity and potential applications, it has been the subject of research in the field of organic chemistry.

6567-11-9

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6567-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6567-11-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6567-11:
(6*6)+(5*5)+(4*6)+(3*7)+(2*1)+(1*1)=109
109 % 10 = 9
So 6567-11-9 is a valid CAS Registry Number.

6567-11-9Downstream Products

6567-11-9Relevant academic research and scientific papers

Asymmetric hydroformylation of deltacyclene

Kollar,Wada,Lautens

, p. 1011 - 1014 (2007/10/02)

Deltacyclene (tetracyclo[4,3,0,02,903,7]non-4-ene was stereoselectively hydroformylated to exo-formyl-deltacyclane in the presence of rhodium and platinum catalysts. In the case of optically active bisphosphines up to 22% e.e-s were achieved.

Convenient method for the production of compounds of the brexane, brendane, and noradamantane series

Gevorkyan, G. G.,Ordubadi, M. D.,Lemma, Tesfaie,Pekhk, T. I.,Belikova, N. A.,et al.

, p. 1736 - 1742 (2007/10/02)

Preparative methods are proposed for the production of 5-brexanone and the acetates of 2-brendanol and 2-noradamantanol from cis-bicyclonona-3,7-diene.Dehydration of 5-brexanol and 2-brendanol gave 4-brexene and deltacyclane respectively.The (13)C NMR spectra of the compounds of the noradamantane, brexane, brendane, and deltacyclane series were studied.

THE BREX-5-YL SYSTEM. A UNIQUELY STRUCTURED NORBORNYL HOMOLOG

Nickon, Alex,Weglein, Raymond C.,Mathew, C. Thomas

, p. 302 - 313 (2007/10/02)

The brexane skeleton functionalized at C-5 is perceived as potentially usefull for various machanistic studies.Our present objective was to prepare and characterize brex-5-yl derivatives and to seek spectroscopic evidence for geometric distortion in the skeleton.The structures synthesized include brex-4-ene, brex-5-one, both of the epimeric brexan-5-ols, and various derivatives of these compounds.Spectroscopic data ( ir, 1H nmr, and uv ) are compared with those from relevant model compounds and are most simply interpreted on the basis of a twist in the brexyl skeleton.This distortion imparts more exocharacter to the C-H bonds at C-4 and more endo character to the C-H bonds at C-5.As an extension of the useful terms geminal and vicinal, we propose the word hominal to represent a 1,3-relationship between two groups.

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