103322-17-4 Usage
Chemical class
Cyclopropane-containing polycyclic aromatic hydrocarbons
Explanation
1H-Cyclopropa[b]naphthalene, 1-(phenylmethylene)is a chemical compound that contains a cyclopropyl ring and multiple aromatic rings.
Explanation
The compound is derived from naphthalene, with a cyclopropyl ring fused to the naphthalene core and a phenylmethylene group (a benzene ring with a double bond) attached to it.
Explanation
Due to its unique structure and chemical properties, 1H-Cyclopropa[b]naphthalene, 1-(phenylmethylene)can be used in the synthesis of new organic compounds, which may lead to the development of novel materials and pharmaceuticals.
Explanation
The combination of a cyclopropyl ring, a phenylmethylene group, and a naphthalene core makes 1H-Cyclopropa[b]naphthalene, 1-(phenylmethylene)- an intriguing subject for further study, as it may exhibit interesting chemical behavior and properties.
Structure
Naphthalene derivative with a cyclopropyl ring and a phenylmethylene substituent
Potential applications
Organic synthesis, new materials, and pharmaceuticals
Unique structure
Interesting and potentially useful molecule for research and development
Check Digit Verification of cas no
The CAS Registry Mumber 103322-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,2 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103322-17:
(8*1)+(7*0)+(6*3)+(5*3)+(4*2)+(3*2)+(2*1)+(1*7)=64
64 % 10 = 4
So 103322-17-4 is a valid CAS Registry Number.
103322-17-4Relevant academic research and scientific papers
Chai, Christina L. L.,Christen, Detlev,Halton, Brian,Neidlein, Richard,Starr, Malcolm A. E.
, p. 577 - 592 (1995)
The behaviour of 1H-cyclopropabenzene (1) and 1H-cyclopropanaphthalene (23) towards a variety of radicals results in opening of the three-membered ring to give ortho-substituted benzyl and 2-methylnaphthalene derivatives, e.g. (13) and (28), respectively.Ring expansion into the cycloheptatriene manifold by way of addition to the bridge bond and norcaradiene formation have not been observed.Analogous reactions with the methylidenecyclopropanaphthalenes (33) and (34) lead to much decomposition, and provide little evidence for the C 1 cycloproparenyl radicals (35) and (36).
Synthetic protocols, molecular polarity, and13C NMR correlations for 1-aryl- and 1-diarylmethylidene-1H-cyclopropa[b]naphthalenes
Halton, Brian,Dixon, Gareth M.
, p. 3139 - 3149 (2007/10/03)
The Peterson olefination for alkylidenecycloproparene synthesis from a 1,1-disilylcycloproparene has been refined into five distinct protocols that have provided 43 new aryl- (5 and 6) and diaryl- (7 and 8). and aryl(phenyl)- (9 and 10) methylidene deriva
