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N,N-bis(2-hydroxyethyl)-2-<(3,4-dimethoxy)phenyl>ethylamine, also known as 2-(3,4-dimethoxyphenyl)-N,N-bis(2-hydroxyethyl)ethylamine, is a complex organic compound with the molecular formula C13H21NO4. It is a derivative of ethylamine, featuring a 3,4-dimethoxyphenyl group attached to the ethylamine backbone. The compound is characterized by two hydroxyethyl groups (-CH2CH2OH) bonded to the nitrogen atom, which contributes to its hydrophilic nature. This chemical structure endows the compound with unique properties, such as potential applications in pharmaceuticals or as a chemical intermediate. The presence of methoxy groups on the phenyl ring can influence its reactivity and solubility, making it a compound of interest in various chemical and biological studies.

4247-65-8

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4247-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4247-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4247-65:
(6*4)+(5*2)+(4*4)+(3*7)+(2*6)+(1*5)=88
88 % 10 = 8
So 4247-65-8 is a valid CAS Registry Number.

4247-65-8Relevant academic research and scientific papers

1,4-(diphenlyalkyl) piperazine derivatives

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, (2008/06/13)

This invention relates to novel compounds of the formula [I], STR1 wherein R 1 and R 2 are the same or different and each represents a lower alkoxy group; A and B are the same or different and each represents a lower alkylene group.The compounds of this i

Synthesis, structure and quantitative structure-activity relationships of σ receptor ligands, 1-[2-(3,4-dimethoxyphenyl)ethyl]-4-(3-phenylpropyl)piperazines

Fujimura, Ken-Ichi,Matsumoto, Junzo,Niwa, Masashi,Kobayashi, Tadayuki,Kawashima, Yoichi,In, Yasuko,Ishida, Toshimasa

, p. 1675 - 1683 (2007/10/03)

A set of the title compounds having different substituents (R1, R2) on their phenyl groups was synthesized to find σ receptor binding affinity. Among the compounds, 2b (R1=R2=Cl) has the most potent σ1-binding activity, while 2a (R1=R2=H, SA4503) was most selective to σ1 over σ2 receptor. The crystal structures of 2a and 2b were shown, by X-ray crystallography, to be similar except for the one torsional angle of their propylene parts. Quantitative structure-activity relationship study suggested the affinity of the compounds to the σ1 receptor was dependent on the electronic feature, Swain-Lupton's R or S(π) that was derived by molecular orbital method, of R1 and R2.

Agent for treatment of disorders of the cerebro-neural transmission system

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, (2008/06/13)

A method for treatment of disorders of the cerebro-neural transmission system which comprises administering a compound of the formula (I) or a pharmaceutically acceptable salt thereof in a therapeutically effective amount, either alone or in admixture wit

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