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1-<2-(1,2,3,4-tetrahydro-2-isoquinolinyl)phenyl>ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124525-67-3

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124525-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124525-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124525-67:
(8*1)+(7*2)+(6*4)+(5*5)+(4*2)+(3*5)+(2*6)+(1*7)=113
113 % 10 = 3
So 124525-67-3 is a valid CAS Registry Number.

124525-67-3Relevant academic research and scientific papers

Intramolecular dehydrative coupling of tertiary amines and ketones promoted by KO-t-Bu/DMF: A new synthesis of indole derivatives

Wei, Wen-Tao,Dong, Xue-Jiao,Nie, Shao-Zhen,Chen, Yan-Yan,Zhang, Xue-Jing,Yan, Ming

, p. 6018 - 6021 (2013)

A new synthesis of indole derivatives has been achieved through intramolecular dehydrative coupling of tertiary amines and ketones promoted by KO-t-Bu/DMF. The reaction probably proceeds via an α-amino alkyl radical pathway.

Diastereoselective synthesis of dihydro-quinolin-4-ones by a borane-catalyzed redox-neutral endo-1,7-hydride shift

Wicker, Garrit,Schoch, Roland,Paradies, Jan

supporting information, p. 3626 - 3630 (2021/05/10)

The borane-catalyzed synthesis of dihydroquinoline-4-ones is developed. The amino-substituted chalcones undergo a 1,7-hydride shift upon Lewis acid activation to form a zwitterionic iminium enolate, which collapses to the dihydroquinoline-4-one scaffold.

Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones

Zhang, Teng,Liang, Weiwei,Huang, Yuxing,Li, Xingrong,Liu, Yizhen,Yang, Bo,He, Chuanxin,Zhou, Xuechang,Zhang, Junmin

supporting information, p. 12536 - 12539 (2017/11/30)

A novel bifunctional organic sponge photocatalyst can enable the efficient coupling of tertiary amines with ketones in water. The asymmetric transformation can be also achieved by using this sponge photocatalyst.

Mild metal-free intramolecular oxidative alkylation of a Csp3-H bond adjacent to a nitrogen atom: A versatile approach to ring-fused tetrahydroquinolines

Zhang, Gen,Wang, Shoulei,Ma, Yunxia,Kong, Weidong,Wang, Rui

supporting information, p. 874 - 879 (2013/05/08)

A metal-free intramolecular oxidative cross-coupling reaction for the constructing Csp3-Csp3 bonds mediated by 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) under mild conditions was realized for the first time. This novel strategy prov

Unprecedented construction of C=C double bonds via Ir-catalyzed dehydrogenative and dehydrative cross-couplings

Nie, Shao-Zhen,Sun, Xiang,Wei, Wen-Tao,Zhang, Xue-Jing,Yan, Ming,Xiao, Jian-Liang

supporting information, p. 2394 - 2397 (2013/06/27)

Unprecedented constructions of C=C double bonds have been achieved by Ir-catalyzed intramolecular dehydrogenative and dehydrative cross-coupling of tertiary amines and ketones. The reactions are proposed to proceed via an Ir-mediated C-H activation mechan

The "tert-amino effect" in heterocyclic chemistry: synthesis of tetra- and pentacyclic compounds

Nijhuis, W. H. N.,Leus, G. R. B.,Egberink, R. J. M.,Verboom, W.,Reinhoudt, D. N.

, p. 172 - 178 (2007/10/02)

A new and covenient route for the synthesis of several heterotetra- and pentacyclic compounds is presented.Heating the 2-vinyl-N,N-dialkylanilines 3a-h, synthesized from the aldehydes 2a-f,h or the acetophenone 2g and malonitrile or ethyl cyanoacetate, in

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