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9H-Cyclohepta[a]naphthalene is a polycyclic aromatic hydrocarbon (PAH) consisting of a seven-membered ring fused to a naphthalene moiety. It is a planar molecule with a molecular formula of C15H12 and a molecular weight of 192.26 g/mol. 9H-Cyclohepta[a]naphthalene is characterized by its unique structure, which features a cycloheptane ring fused to one of the naphthalene rings. 9H-Cyclohepta[a]naphthalene is known for its potential applications in organic synthesis and as a precursor in the production of various pharmaceuticals and materials. However, due to its complex structure and limited availability, it is not as widely studied as other PAHs. Nonetheless, it remains an interesting target for researchers in the field of organic chemistry and materials science.

231-64-1

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231-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 231-64-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 231-64:
(5*2)+(4*3)+(3*1)+(2*6)+(1*4)=41
41 % 10 = 1
So 231-64-1 is a valid CAS Registry Number.

231-64-1Downstream Products

231-64-1Relevant academic research and scientific papers

1,7-Electrocyclisation and Carbene Reactions of o-Alkenylaryldiazoalkanes: The Effect of Alkene Configuration on the Mode of Reaction

Munro, David P.,Sharp, John T.

, p. 849 - 858 (2007/10/02)

The 1,7-8?-electron electrocyclisation of o-alkenylaryldiazoalkanes (1) to give 1H-2,3-benzodiazepines (3) takes place readily for substrates with a cis-hydrogen atom at the cyclisation site, but is blocked by phenyl or methyl groups at that position.Such

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