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N-(4-chlorobenzyl)-2-aminonaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97306-78-0

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97306-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97306-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,0 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97306-78:
(7*9)+(6*7)+(5*3)+(4*0)+(3*6)+(2*7)+(1*8)=160
160 % 10 = 0
So 97306-78-0 is a valid CAS Registry Number.

97306-78-0Downstream Products

97306-78-0Relevant academic research and scientific papers

Mechanistic Insights into the FeCl3-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes

Vershinin, Vlada,Forkosh, Hagit,Ben-Lulu, Mor,Libman, Anna,Pappo, Doron

, p. 79 - 90 (2020/12/23)

The selective FeCl3-catalyzed oxidative cross-coupling reaction between phenols and primary, secondary, and tertiary 2-aminonaphthalene derivatives was investigated. The generality of this scalable method provides a sustainable alternative for preparing N,O-biaryl compounds that are widely used as ligands and catalysts. Based on a comprehensive kinetic investigation, a catalytic cycle involving a ternary complex that binds to both the coupling partners and the oxidant during the key oxidative coupling step is postulated. Furthermore, the studies showed that the reaction is regulated by off-cycle acid-base and ligand exchange processes.

Design and Atroposelective Construction of IAN analogues by Organocatalytic Asymmetric Heteroannulation of Alkynes

Shen, Jiahua,Tan, Bin,Wang, Yong-Bin,Wu, San,Zhang, Lei,Zhong, Guofu

supporting information, p. 23077 - 23082 (2020/10/19)

An organocatalytic atroposelective strategy for accessing enantioenriched axially chiral IAN analogues was developed for the first time. A class of novel atropisomeric C2-arylquinoline skeletons were synthesized with high enantiocontrol via chiral phosphoric-acid-catalyzed heteroannulation of in situ generated vinylidene ortho-quinone methide (VQM) intermediates with ortho-aminophenones. The strategy tolerated a broad substrate scope, providing a facile organocatalytic approach to IAN analogues in good yields and excellent enantioselectivities under mild reaction conditions. Moreover, the synthetic utility of this methodology was illustrated through further transformations into IAN-type ligand and axially chiral thiourea.

Method for catalytical asmmytrical synthesis of binaphthyldiamine

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Paragraph 0054; 0061-0064; 0086-0088, (2019/04/04)

The invention belongs to the field of asmmytric synthesis and discloses a method for catalytical asmmytrical synthesis of binaphthyldiamine. The method comprises the following steps of by taking metaltriflates and a chiral bisoxazoline ligand as catalysts

SYNTHESIS AND SPECTRAL CHARACTERISTICS OF ACENAPHTHENE DERIVATIVES OF BENZOQUINOLINE

Kozlov, N. S.,Shmanai, G. S.,Dang Ny Tai

, p. 894 - 898 (2007/10/02)

The catalytic interaction of 5-acetylacenaphthene with arylidene-2-naphthylamines leads to the formation of adduct to the C=N bond (aminoketones) or 1-(5-acenaphthenyl)-3-aryl-heteroaryl)benzoquinolines.In several instances they are accompanied by 1-(5

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