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10,11-Dihydro-5,10-ethano-5H-dibenzo[a,d]cyclohepten-11-one is a complex organic compound with the molecular formula C17H16O. It is a derivative of dibenzocyclohepten, a type of tricyclic aromatic compound. This specific compound features a cycloheptenone ring fused to two benzene rings, with an ethano bridge connecting the 5 and 10 positions. The 10,11-dihydro functional group indicates the presence of a double bond between carbons 10 and 11, which has been reduced to a single bond, and an additional hydrogen atom is attached to carbon 11. 10,11-Dihydro-5,10-ethano-5H-dibenzocyclohepten-11-one is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and properties.

24330-03-8

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24330-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24330-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24330-03:
(7*2)+(6*4)+(5*3)+(4*3)+(3*0)+(2*0)+(1*3)=68
68 % 10 = 8
So 24330-03-8 is a valid CAS Registry Number.

24330-03-8Upstream product

24330-03-8Downstream Products

24330-03-8Relevant academic research and scientific papers

FLOW-VACUUM PYROLYSIS OF POLYCYCLIC COMPOUNDS. PYROLYSIS OF EXO-10,11-DIHYDRO-5,10-ETHANO-5H-DIBENZOCYCLOHEPTEN-11-YL ACETATE AND EXO-10,11-DIHYDRO-5,10-ETHANO-5H-DIBENZOCYCLOHEPTEN-11-OL

Stanescu, Michaela Dina,Florea, Cristina,Banciu, Mircea D.

, p. 815 - 820 (2007/10/02)

The flow-vacuum pyrolyses of the title compounds 2, respectively 1, were performed between 300 deg C and 675 deg C (650 deg C), at 1 Torr.The results are discussed in comparison with those obtained in the previously described pyrolyses of the corresponding endo-isomers 5, respectively 4.

FLOW-VACUUM PYROLYSIS OF POLYCYCLIC COMPOUNDS. 3. FLOW-VACUUM PYROLYSIS OF endo-10,11-DIHYDRO-5,10-ETHANO-5H-DIBENZOCYCLOHEPTEN-11-YL ACETATE AND OF endo-10,11-DIHYDRO-5,10-ETHANO-5H-DIBENZOCYCLOHEPTEN-11-OL

Banciu, Mircea D.,Stanescu, Michaela Dina,Florea, Cristina,Petride, Aurica,Cioranescu, Ecaterina

, p. 1211 - 1218 (2007/10/03)

The flow-vacuum pyrolyses of title compounds 6 and 7 were examined at 1 Torr and various temperatures between 250 deg C (respectively 300 deg C) and 650 deg C. From both pyrolyses the following hydrocarbons were formed: 9,10-dihydro-9,10-propenoanthracene (1), 1,1a,6,10b-tetrahydro-1,6-methano-dibenzocyclopropacycloheptene (2), 11,11a-dihydro-6aH-benzofluorene (3), 6,11-dihydro-5H-benzofluorene (4), 11H-benzofluorene (5) and anthracene. Besides these products the epimeric exo-acetate 10 was formed in pyrolysis of endo-acetate 6 whereas from pyrolysis of 7 important amounts of corresponding ketone 9 were obtained. A radical mechanism is suggested.

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