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((2R,4R)-2,6-Dimethyl-1,2,3,4-tetrahydro-quinolin-4-yl)-p-tolyl-amine is a complex organic compound with a molecular formula of C18H22N2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific 2R,4R configuration. ((2R,4R)-2,6-Dimethyl-1,2,3,4-tetrahydro-quinolin-4-yl)-p-tolyl-amine features a tetrahydroquinoline ring system, which is a partially saturated derivative of quinoline, and is substituted with two methyl groups at the 2 and 6 positions. The molecule also includes a p-tolyl group, which is a para-methylphenyl group, attached to the nitrogen atom. ((2R,4R)-2,6-Dimethyl-1,2,3,4-tetrahydro-quinolin-4-yl)-p-tolyl-amine is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or other chemical industries due to its unique structure and properties.

22609-18-3

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22609-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22609-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,0 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22609-18:
(7*2)+(6*2)+(5*6)+(4*0)+(3*9)+(2*1)+(1*8)=93
93 % 10 = 3
So 22609-18-3 is a valid CAS Registry Number.

22609-18-3Relevant academic research and scientific papers

Radical cation salt induced tandem cyclization between anilines and N-vinyl amides: Synthesis of 2-methyl-4-anilino-1,2,3,4-tetrahydroquinoline derivatives

Jia, Xiao-Dong,Ren, Yan,Huo, Cong-De,Wang, Wen-Juan,Chen, Xiang-Ning,Xu, Xiao-Lan,Wang, Xi-Cun

, p. 6779 - 6782 (2010)

A tandem cyclization of imines with N-vinyllactams induced by TBPA + was investigated, and a series of 2-methyl-4-anilino-1,2,3,4- tetrahydroquinolines were synthesized based on a domino process in which N-vinyllactams serve as an acetaldehyde

Sequential Photoredox Catalysis for Cascade Aerobic Decarboxylative Povarov and Oxidative Dehydrogenation Reactions of N-Aryl α-Amino Acids

Shao, Tianju,Yin, Yanli,Lee, Richmond,Zhao, Xiaowei,Chai, Guobi,Jiang, Zhiyong

supporting information, p. 1754 - 1760 (2018/03/21)

A visible-light-driven sequential photoredox catalysis to allow N-aryl α-amino acids to experience efficient cascade aerobic decarboxylative Povarov and oxidative dehydrogenation (ODH) reactions is described. With a dicyanopyrazine-derived chromophore (DP

Method for synthesizing 1,2,3,4-tetrahydroquinoline compounds in mode that decarboxylation of amino acid is catalyzed by visible light

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Paragraph 0011; 0013; 0014, (2018/05/30)

The invention relates to a method for synthesizing 1,2,3,4-tetrahydroquinoline compounds in the mode that decarboxylation of amino acid is catalyzed by visible light. The method is characterized in that in an air atmosphere, the N-phenyl amino acidic compounds shown in the formula I, an organic photocatalyst DPZ and 4-molecular sieve are dissolved in an organic solvent, stirred and reacted for atleast 5 hours at the temperature of 20-30 DEG C under the irradiation of the visible light, separation and purification are conducted, and then the tetrahydroquinoline compounds shown in the formula II are obtained, wherein in the formula I and the formula II (the formulas are shown in the description), R is representative for any one of hydrogen, halogen, alkyl, phenyl and alkoxy, R1 is representative for any one of hydrogen, methyl, n-propyl and phenyl, alkyl is representative for methyl or ethyl or normal-butyl or benzyl, and aryl is representative for substituted phenyl or 4-tert-butyl phenyl. According to the method, substrates are simple, reaction conditions are mild, the usage amount of the catalyst is low, the yield is high, and no metal participates in a reaction.

COMPOUNDS AND MATRICES FOR USE IN BONE GROWTH AND REPAIR

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Paragraph 0333;0340;0341, (2016/03/05)

Compositions of small molecules, matrices, and isolated cells including methods of preparation, and methods for differentiation, transdifferentiation, and proliferation of animal cells into the osteoblast blast cell lineage were described. Examples of ost

Efficient bromination of polyaniline base to poly(2-bromoaniline)-bromide salt and its application as a recyclable catalyst for the synthesis of 2-methyl-4-anilino-1,2,3,4-tetrahydroquinolines

Rajender, Boddula,Palaniappan, Srinivasan

, p. 94 - 98 (2014/10/15)

Efficient bromination of polyaniline base to poly(2-bromoaniline)-bromide is successfully carried out using bromodimethylsulfonium bromide. Poly(2-bromoaniline)-bromide salt was obtained in a dry amorphous nature, having high conductivity (2.5 S/cm) with

Efficient bromination of polyaniline base to poly(2-bromoaniline)-bromide salt and its application as a recyclable catalyst for the synthesis of 2-methyl-4-anilino-1,2,3,4-tetrahydroquinolines

Rajender, Boddula,Palaniappan, Srinivasan

, p. 94 - 98 (2016/10/25)

Efficient bromination of polyaniline base to poly(2-bromoaniline)-bromide is successfully carried out using bromodimethylsulfonium bromide. Poly(2-bromoaniline)-bromide salt was obtained in a dry amorphous nature, having high conductivity (2.5 S/cm) with

Synthesis and SAR of cis-1-Benzoyl-1,2,3,4-tetrahydroquinoline ligands for control of gene expression in ecdysone responsive systems

Smith, Howard C.,Cavanaugh, Caitlin K.,Friz, Jennifer L.,Thompson, Christine S.,Saggers, Jessica A.,Michelotti, Enrique L.,Garcia, Javier,Tice, Colin M.

, p. 1943 - 1946 (2007/10/03)

A library of 35 cis-1-benzoyl-2-methyl-4-(phenylamino)-1,2,3,4-tetrahydroquinolines was prepared. The compounds bore various substitutuents on the benzoyl ring, at the 4-position of the phenylamino ring and at the 6-position of the tetrahydroquinoline rin

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