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5-Benzyl-5,11-dihydro-6H-dibenzo[b,e]azepin-6-one is a complex organic chemical compound belonging to the class of dibenzazepine derivatives. It is characterized by a unique molecular structure, featuring a benzene ring fused to an azepine ring, with a benzyl group attached at the 5-position and a ketone functional group at the 6-position. 5-benzyl-5,11-dihydro-6H-dibenzo[b,e]azepin-6-one is primarily of interest in the field of medicinal chemistry, as it may exhibit potential therapeutic properties or serve as a precursor in the synthesis of other bioactive molecules. Its chemical formula is C18H17NO, and it has a molecular weight of 263.33 g/mol. The compound's structure and properties make it a subject of study for researchers exploring the development of new drugs and pharmaceuticals.

3311-41-9

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3311-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3311-41-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,1 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3311-41:
(6*3)+(5*3)+(4*1)+(3*1)+(2*4)+(1*1)=49
49 % 10 = 9
So 3311-41-9 is a valid CAS Registry Number.

3311-41-9Relevant academic research and scientific papers

A Modular Approach to Dibenzo-fused ?-Lactams: Palladium-Catalyzed Bridging-C?H Activation

Huang, Xueliang,Ma, Liyao,Xia, Jiajin,Xin, Luoting,Yu, Yinghua,Zhu, Lei

supporting information, p. 18261 - 18266 (2020/08/21)

Tricyclic ring systems possessing a dibenzo structure joined to a seven-membered heterocyclic ring frequently show important biological activities. However, a modular approach to these molecules based on efficient intermolecular reaction of readily available chemicals is lacking. Herein, an unprecedented palladium-catalyzed formal [4+3] annulation for modular construction of these tricyclic systems is described. This reaction features easily accessible reactants (o-haloarylaldehydes and N-tosylhydrazones), broad substrate scope, and excellent functional group compatibility. The synthetic potential is demonstrated by the easy scale-up reactions, late-stage modification of complex molecules, and collective synthesis of bioactive molecules and approved drugs.

OXYDATION OF TERTIARY POLYCYCLIC AMINES BY RuO4

Bettoni, Giancarlo,Carbonara, Giuseppe,Franchini, Carlo,Tortorella, Vincenzo

, p. 4159 - 4164 (2007/10/02)

The reactions of certain tertiary polycyclic amines such as N-benzyl-9-azabicyclo--nonane, N-benzyl-5,6-dihydro-11H-dibenzazepine, and N-benzyl-1,2,3,4-tetrahydroisoquinoline with ruthenium tetroxide, taking place in both heterogeneous and hom

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