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10-(4-methoxybenzyl)-9,10-dihydroacridine is a chemical compound with the molecular formula C20H19NO2. It is a derivative of the acridine family, characterized by a tricyclic structure with a dihydroacridine ring system. The compound features a 4-methoxybenzyl group attached to the 10th position of the acridine core, which introduces a methoxy (-OCH3) functional group to the molecule. This modification can significantly influence the compound's physical, chemical, and biological properties, potentially affecting its solubility, stability, and interactions with biological targets. The compound may be of interest in medicinal chemistry and drug development due to the diverse pharmacological activities associated with acridine derivatives, including their potential as antimalarial, antiviral, and anticancer agents.

87742-31-2

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87742-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87742-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,4 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87742-31:
(7*8)+(6*7)+(5*7)+(4*4)+(3*2)+(2*3)+(1*1)=162
162 % 10 = 2
So 87742-31-2 is a valid CAS Registry Number.

87742-31-2Relevant academic research and scientific papers

Metal-free TEMPO-catalyzed oxidative C-C bond formation from Csp 3-H bonds using molecular oxygen as the oxidant

Zhang, Bo,Cui, Yuxin,Jiao, Ning

, p. 4498 - 4500 (2012/06/01)

An efficient TEMPO-catalyzed oxidative C-C bond formation with two Csp 3-H bonds using molecular oxygen as the oxidant has been developed. The novel transformation provides a new strategy for the TEMPO-O2 catalysis to construct C-C bonds. The advantages of this method include: (1) relatively mild and neutral conditions; (2) simplicity and safety of operation; (3) a stoichiometric amount of dangerous oxidants, any transition metals, additives, even solvent, is not required.

Hydride transfer reactions. Substituent effects in oxidation of N-benzylacridans by ? acceptors

Colter, Allan K.,Lai, Charles C.,Williamson, Terry W.,Berry, Raymond E.

, p. 2544 - 2551 (2007/10/02)

The kinetics of oxidation of a series of eight N-(substituted benzyl)acridans (3, NBA's) by 1,4-benzoquinone (BQ), p-chloranil (CA), 2,3-dicyano-1,4-benzoquinone (DCBQ), 7,7,8,8-tetracyanoquinodimethane (TCNQ), and tetracyanoethylene (TCNE) in acetonitril

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