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1,4-dihydroxy-2-(piperidin-1-yl)anthracene-9,10-dione is a complex organic compound with a molecular formula of C22H21NO4. It is characterized by the presence of two hydroxyl groups at the 1st and 4th carbon positions, a piperidin-1-yl group attached to the 2nd carbon, and a 9,10-dione functional group. 1,4-dihydroxy-2-(piperidin-1-yl)anthracene-9,10-dione is a derivative of anthracene, a tricyclic aromatic hydrocarbon, and exhibits a unique structure that may have potential applications in various fields, such as pharmaceuticals, dyes, or materials science. Due to its specific functional groups and molecular structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest for researchers in organic chemistry.

4644-02-4

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4644-02-4 Usage

Chemical structure

1,4-dihydroxy-2-(piperidin-1-yl)anthracene-9,10-dione is an anthracene derivative with a piperidine ring attached to the 2nd position and hydroxyl groups at the 1st and 4th positions.

Molecular weight

Approximately 353.38 g/mol

Functional groups

Hydroxyl (-OH), carbonyl (C=O), and piperidine (heterocyclic amine)

Appearance

Yellow to orange crystalline solid

Solubility

Soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO)

Stability

Stable under normal laboratory conditions, but sensitive to light and heat

Reactivity

Can undergo various chemical reactions such as oxidation, reduction, and substitution due to the presence of functional groups

Synthesis

Prepared through the reaction of anthracene-9,10-dione with a suitable piperidine derivative in the presence of a catalyst or reagent

Pharmaceutical intermediate

Used in the synthesis of various pharmaceuticals and organic compounds

Medicinal chemistry

Potential applications in the field of medicinal chemistry due to its ability to interact with biological targets and modulate their activity

Fluorescent dye

May have potential use as a fluorescent dye due to its anthracene core

Building block

Can be used as a building block for the construction of more complex organic molecules

Biological properties

Interaction with biological targets and modulation of their activity, which may lead to potential therapeutic applications

Research and industrial applications

Valuable compound for various research and industrial applications due to its chemical and biological properties

Check Digit Verification of cas no

The CAS Registry Mumber 4644-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,4 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4644-02:
(6*4)+(5*6)+(4*4)+(3*4)+(2*0)+(1*2)=84
84 % 10 = 4
So 4644-02-4 is a valid CAS Registry Number.

4644-02-4Downstream Products

4644-02-4Relevant academic research and scientific papers

Synthesis of Dimeric and cyclo-Trimeric 1,4-Anthraquinones

Laatsch, Hartmut

, p. 839 - 858 (2007/10/02)

By phenol/quinone addition, similar to the parent compound 1, substituted 1,4-anthraquinones form dimers and cyclo-trimers; the latter are potentially chiral.Key intermediate in the synthesis of cyclo-triquinizarine (16b) is the ether 19b which shows strong triboluminescence and phosphorescence.

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