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10-phenyl-1,2,3,4-tetrahydrophenanthrene is an organic compound with a molecular formula of C21H20. It is a derivative of phenanthrene, a polycyclic aromatic hydrocarbon, and features a phenyl group attached to the 10th carbon atom of the tetrahydrophenanthrene structure. 10-phenyl-1,2,3,4-tetrahydrophenanthrene is characterized by its unique molecular arrangement, which consists of a central phenanthrene core with four hydrogen atoms attached to the carbon atoms at positions 1, 2, 3, and 4, and a phenyl ring connected to the 10th carbon. Due to its complex structure, 10-phenyl-1,2,3,4-tetrahydrophenanthrene has potential applications in various fields, such as pharmaceuticals, materials science, and chemical research. However, it is essential to consider its potential environmental and health impacts, as many polycyclic aromatic hydrocarbons are known to be toxic and carcinogenic.

844-19-9

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844-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 844-19-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 844-19:
(5*8)+(4*4)+(3*4)+(2*1)+(1*9)=79
79 % 10 = 9
So 844-19-9 is a valid CAS Registry Number.

844-19-9Downstream Products

844-19-9Relevant academic research and scientific papers

Sequential Suzuki-Miyaura Coupling/Lewis Acid-Catalyzed Cyclization: An Entry to Functionalized Cycloalkane-Fused Naphthalenes

Mahecha-Mahecha, Camilo,Lecornué, Frédéric,Akinari, Sumita,Charote, Thomas,Gamba-Sánchez, Diego,Ohwada, Tomohiko,Thibaudeau, Sébastien

, p. 6267 - 6271 (2020)

Functionalized angular cycloalkane-fused naphthalenes were prepared using a two-step process involving a Pd-catalyzed Suzuki-Miyaura coupling of aryl pinacol boronates and vinyl triflates followed by a boron trifluoride etherate-catalyzed cycloaromatization.

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