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6-p-toluenesulfonyl-6,7-dihydro-5H-dibenz[c,e]azepine is a complex organic chemical compound with the molecular formula C17H17NOS. It is a derivative of dibenzazepine, a tricyclic aromatic compound with a seven-membered ring. The molecule features a toluenesulfonyl group (a sulfonyl group derived from toluene) attached to the 6-position of the dibenzazepine core. 6-p-toluenesulfonyl-6,7-dihydro-5H-dibenz[c,e]azepine is of interest in the field of medicinal chemistry, particularly in the development of potential therapeutic agents, due to its unique structure and the ability to form various interactions with biological targets. It is important to note that the specific properties, applications, and safety considerations of 6-p-toluenesulfonyl-6,7-dihydro-5H-dibenz[c,e]azepine would require further investigation and are not detailed in this brief summary.

1924-75-0

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1924-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1924-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1924-75:
(6*1)+(5*9)+(4*2)+(3*4)+(2*7)+(1*5)=90
90 % 10 = 0
So 1924-75-0 is a valid CAS Registry Number.

1924-75-0Downstream Products

1924-75-0Relevant academic research and scientific papers

Palladium-catalyzed (Ullmann-type) homocoupling of aryl halides: A convenient and general synthesis of symmetrical biaryls via inter- and intramolecular coupling reactions

Hennings, D. David,Iwama, Tetsuo,Rawal, Viresh H.

, p. 1205 - 1208 (1999)

(matrix presented) A convenient new procedure is described for both inter-and intramolecular homocoupling of aryl halides (Ullmann reaction) using catalytic palladium in the presence of hydroquinone, a homogeneous reductant. Optimal conditions for the reductive coupling include the use of a 1:1 molar ratio of Pd(OAc)2 and As(o-tolyl)3 in catalytic amounts under basic conditions.

Palladium-catalyzed regiocontrolled domino synthesis of N-sulfonyl dihydrophenanthridines and dihydrodibenzo[c, e]azepines: Control over the formation of biaryl sultams in the intramolecular direct arylation

Laha, Joydev K.,Dayal, Neetu,Jain, Roli,Patel, Ketul

, p. 10899 - 10907 (2015/01/08)

A palladium-catalyzed domino N-benzylation/intramolecular direct arylation involving sulfonanilides and 2-bromobenzyl bromides has been developed for the first time, providing a workable access to N-sulfonyl dihydrophenanthridines in good to excellent yields. Under the optimized conditions, the formation of 5,6-dihydrophenanthridines was largely controlled over the formation of biaryl sultams containing a seven member ring. The optimized condition was found extendable to the regiocontrolled domino formation of N-sulfonyl-6,7-dihydro-5H-dibenzo[c,e]azepines over the biaryl sultam formation. Using an appropriate substrate, a biaryl sultam has been obtained exclusively.

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