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2-(benzo[d][1,3]dioxol-5-yl)-N-(3,4-dimethoxyphenethyl)ethan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1194765-46-2

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1194765-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1194765-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,7,6 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1194765-46:
(9*1)+(8*1)+(7*9)+(6*4)+(5*7)+(4*6)+(3*5)+(2*4)+(1*6)=192
192 % 10 = 2
So 1194765-46-2 is a valid CAS Registry Number.

1194765-46-2Downstream Products

1194765-46-2Relevant academic research and scientific papers

New halogenated tris-(phenylalkyl)amines as h5-HT2Breceptor ligands

Kapadia, Nirav,Ahmed, Shahrear,Harding, Wayne W.

, p. 3216 - 3219 (2016)

A series of compounds in which various halogen substituents were incorporated into a phenyl ring of a tris-(phenylalkyl)amine scaffold, was synthesized and evaluated for affinity to h5-HT2receptors. In general, all compounds were found to have

Identification of tris-(phenylalkyl)amines as new selective h5-HT2B receptor antagonists

Ponnala, Shashikanth,Kapadia, Nirav,Harding, Wayne Wesley

, p. 601 - 605 (2015/04/27)

A series of tris-(phenylalkyl)amines was synthesized and evaluated for affinity to human 5-HT2 receptors. In general, the compounds displayed high affinity (4 of 11 analogs had Ki values 2B receptor vs. other 5-HT2 receptors. Functional assays revealed that the compounds are 5-HT2B antagonists. This journal is

(±)-Nantenine analogs as antagonists at human 5-HT2A receptors: C1 and flexible congeners

Chaudhary, Sandeep,Pecic, Stevan,LeGendre, Onica,Navarro, Hérnan A.,Harding, Wayne W.

scheme or table, p. 2530 - 2532 (2009/12/25)

C1 and flexible analogs of (±)-nantenine were synthesized and evaluated for antagonist activity at human 5-HT2A receptors in a calcium mobilization assay. This work has resulted in the identification of the most potent 5-HT2A antagon

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