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9,10,11,11a-Tetrahydrobenzo[b]naphtho[1,2-d]furan-7a(8H)-ol is a complex organic compound belonging to the class of polycyclic aromatic hydrocarbons. It is characterized by a unique molecular structure, featuring a benzene ring fused to a naphthalene core, with an additional furan ring and a hydroxyl group at the 7a position. 9,10,11,11a-tetrahydrobenzo[b]naphtho[1,2-d]furan-7a(8H)-ol is of interest in the field of organic chemistry, particularly for its potential applications in pharmaceuticals and materials science. Its chemical properties, such as reactivity and stability, are influenced by the presence of the hydroxyl group and the overall structure, which can lead to various functional groups and interactions with other molecules. The compound's specific applications and effects are subject to ongoing research, as its complex structure offers a range of possibilities for chemical modification and potential therapeutic uses.

6320-06-5

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6320-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6320-06-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6320-06:
(6*6)+(5*3)+(4*2)+(3*0)+(2*0)+(1*6)=65
65 % 10 = 5
So 6320-06-5 is a valid CAS Registry Number.

6320-06-5Relevant academic research and scientific papers

Efficient catalytic-free method to produce α-aryl cycloalkanones through highly chemoselective coupling of aryl compounds with oxyallyl cations

Luo, Juan,Zhou, Hui,Hu, Jiwei,Wang, Rui,Tang, Qiang

, p. 17370 - 17377 (2014/05/06)

Catalytic-free coupling of aryl compounds and α-halo cycloketones via in situ generated oxyallyl cation intermediates is reported here. The reactions efficiently afford α-naphthol cycloalkanones with moderate to excellent yields. Electron-rich aromatic compounds are also used to produce the corresponding α-aryl cycloalkanones, and in some cases, analytically pure products are obtained after simple filtration followed by evaporation.

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