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1-(2-(4-(tert-butyl)phenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-propan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1402732-48-2

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1402732-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402732-48-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,7,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1402732-48:
(9*1)+(8*4)+(7*0)+(6*2)+(5*7)+(4*3)+(3*2)+(2*4)+(1*8)=122
122 % 10 = 2
So 1402732-48-2 is a valid CAS Registry Number.

1402732-48-2Downstream Products

1402732-48-2Relevant academic research and scientific papers

Carbon nitride-catalyzed photoredox C-C bond formation with N-aryltetrahydroisoquinolines

Moehlmann, Lennart,Baar, Moritz,Riess, Julian,Antonietti, Markus,Wang, Xinchen,Blechert, Siegfried

, p. 1909 - 1913 (2012)

In this communication we describe the oxidative C-C bond formation of tertiary amines with various nucleophiles under very mild and environmental friendly conditions by using mesoporous graphitic carbon nitride (mpg-C 3N4) semiconduc

The Photocatalyst-Free Cross-Dehydrogenative Coupling Reaction Enabled by Visible-Light Direct Excitation of Substrate

Guo, Xuan,Shao, Bing-Ru,Jiang, Wen-Feng,Shi, Lei

, p. 15743 - 15752 (2021/11/16)

A new photocatalyst-free strategy for the cross-dehydrogenative C-C and C-P coupling reaction has been described. This protocol provides a concise method to synthesize various 1-substituted tetrahydroisoquinoline (THIQ) derivatives enabled by visible-ligh

Carbazole-triazine based donor-acceptor porous organic frameworks for efficient visible-light photocatalytic aerobic oxidation reactions

Luo, Jian,Lu, Jingzhi,Zhang, Jian

supporting information, p. 15154 - 15161 (2018/08/17)

We report the synthesis of a series of carbazole-triazine based donor-acceptor (D-A) POFs and their photocatalytic activities for aerobic oxidation reactions. The simultaneous introduction of a carbazole-based electron donor and a triazine-based electron acceptor in D-A POFs stabilizes the charge transfer state and enables an efficient triplet-triplet energy transfer to generate 1O2. Meanwhile, systematic variation of the D-A distance results in the tunable photoredox properties and consequently the efficiency for generation of reactive oxygen species (ROSs). Upon visible light excitation, all three D-A POFs exhibit excellent capability to promote three aerobic oxidations: sulfide oxidation, oxidative amine coupling, and Mannich reactions. This systematic study validates the design principle of D-A POFs as high-performance photo-oxidation catalysts with wide substrate scope and excellent stability and recyclability.

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