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Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-[4-(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

596788-79-3

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596788-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596788-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,7,8 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 596788-79:
(8*5)+(7*9)+(6*6)+(5*7)+(4*8)+(3*8)+(2*7)+(1*9)=253
253 % 10 = 3
So 596788-79-3 is a valid CAS Registry Number.

596788-79-3Relevant academic research and scientific papers

1-Aryl-tetrahydroisoquinoline analogs as active anti-HIV agents in vitro

Cheng, Pi,Huang, Ning,Jiang, Zhi-Yong,Zhang, Quan,Zheng, Yong-Tang,Chen, Ji-Jun,Zhang, Xue-Mei,Ma, Yun-Bao

, p. 2475 - 2478 (2008/09/20)

A series of 1-aryl-6,7-dihydroxyl(methoxy)-1,2,3,4-tetrahydroisoquinolines (compounds 1-36) were synthesized via Pictet-Spengler cyclization. All the synthesized compounds were assayed for activities against HIV-1IIIB in C8166 cell cultures by

Synthesis of benzoazocines from substituted tetrahydroisoquinolines and activated alkynes in a tetrahydropyridine ring expansion

Voskressensky, Leonid G.,Listratova, Anna V.,Borisova, Tatiana N.,Alexandrov, Grigoriy G.,Varlamov, Alexey V.

, p. 6106 - 6117 (2008/09/17)

Tetrahydroisoquinolines underwent tandem piperidine ring enlargement in the presence of activated alkynes in acetonitrile or methanol, producing tetrahydrobenzo[d]azocines in high yields. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

Tandem enlargement of the tetrahydropyridine ring in 1-aryl-tetrahydroisoquinolines using activated alkynes-a new and effective synthesis of benzoazocines

Voskressensky, Leonid G.,Borisova, Tatiana N.,Listratova, Anna V.,Kulikova, Larisa N.,Titov, Alexander A.,Varlamov, Alexey V.

, p. 4585 - 4589 (2007/10/03)

Tetrahydroisoquinolines 3a-e underwent piperidine ring enlargement under the action of activated alkynes, giving benzoazocines 4, 5 and 7-11 in high yields.

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