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Usage

Synthetic organic compound

Derived from anthracene 2,3-bis(bromomethyl)-1,4-dihydroxyanthracene-9,10-dione is a synthetic organic compound, meaning it is man-made and not found naturally in the environment. It is derived from anthracene, which is a polycyclic aromatic hydrocarbon.

Dihydroxyanthracenedione derivative

Contains two hydroxyl groups 2,3-bis(bromomethyl)-1,4-dihydroxyanthracene-9,10-dione is a derivative of dihydroxyanthracenedione, which means it contains two hydroxyl (OH) groups in its structure.

Bromomethyl groups

Attached to the 2 and 3 positions of the anthracene ring The compound has two bromomethyl (CH2Br) groups attached to the 2 and 3 positions on the anthracene ring, which is the central structure of the compound.

Physical appearance

Yellow to orange crystalline powder 2,3-bis(bromomethyl)-1,4-dihydroxyanthracene-9,10-dione is a yellow to orange crystalline powder, which means it has a solid, crystalline structure with a yellow to orange color.

Industrial applications

Production of dyes and pigments 2,3-bis(bromomethyl)-1,4-dihydroxyanthracene-9,10-dione is used in the production of dyes and pigments, which are coloring agents used in various industries, such as paint, ink, and plastics.

Medicinal potential

Pharmaceuticals and biological research Due to its chemical structure, 2,3-bis(bromomethyl)-1,4-dihydroxyanthracene-9,10-dione may have potential medicinal uses, such as in the development of pharmaceuticals or in biological research.

Upstream product

• 608-43-5 2,3-dimethyl-1,4-dihydroxybenzene 
• 17850-83-8 2,3-dimethylanthracene-1,4,9,10-tetraone 
• 85-44-9 phthalic anhydride 
• 25060-18-8 2,3-dimethyl quinizarine 

Downstream Products

• 67122-26-3 2-acetyl-1,2,3,4,6,11-hexahydro-5,12-dihydroxynaphthacene-6,11-quinone 
• 77422-63-0 C₃₂H₂₀O₈ 
• 89024-03-3 (3aS,13aR)-5,12-Dihydroxy-2-phenyl-3a,4,13,13a-tetrahydro-2-aza-cyclopenta[b]naphthacene-1,3,6,11-tetraone 

Relevant academic research and scientific papers

Influence of silver nanoparticles on 2,3-Bis(Chloromethyl)anthracene-1,4,9, 10-tetraone

Size effect of silver nano particles on the photophysical properties of 2,3-bis(chloromethyl)anthracene-1,4,9,10-tetraone (BCMAT) have been investigated using optical absorption and fluorescence emission techniques. Silver NPs of different sizes have been prepared by two different methods. Quenching of fluorescence of BCMAT has been found to increase with decrease in the size of the silver NPs. Stern-Volmer quenching constants have also been calculated.

Synthesis and characterisation of C60 derivatives containing functionalised anthraquinone groups and an unusual fullerene-stabilised cation

The ortho-anthraquinonedimethane dienophiles prepared in situ from 1,4-dihydroxy-2,3-bis(bromomethyl)-anthraquinone and 1,4-dimethoxy-2,3-bis(bromomethyl)anthraquinone respectively react with the fullerene C60 to give the anthraquinone derivatives: dihydroxy-anthraquinone-C60 and dimethoxy-anthraquinone-C60. The former compound with sodium butoxide and 15-crown-5 gives the bis(sodium-15-crown-5)dioxo-anthraquinone-C60. The dimethoxy-anthraquinone-C60 reacts with [Ru(PPh3)2(NO)Cl] to form the bis-adduct {[η2-(dimethoxy-anthraquinone-C60)][Ru(PPh3 )2(NO)Cl]}. The electrochemistry of the dihydroxy- and dimethoxy-anthraquinone-C60 derivatives has been studied by cyclic voltammetry and, in contrast to 1,4-dihydroxy-2,3-dimethylanthraquinone, the compound dihydroxy-anthraquinone-C60 shows two separate one electron oxidations at lower potentials strongly suggesting a relatively rare example of a fullerene stablised cation.

3-(Acyloxy)-3-buten-2-ones as Dienophiles in Anthracyclinone Synthesis. An Efficient Route to 4-Demethoxy-7-deoxydaunomycinone Derivatives.

Biacetyl has been converted into a series of 3-(acyloxy)-3-buten-2-ones (13-17) which were characterized both spectroscopically and as their crystalline adducts with 1,3-diphenylisobenzofuran.A comparative study has been made of the reaction of these dien

Simple o-Quinodimethane Route to (+/-)-4-Demethoxydaunomycinone

The anthracycline antibiotics daunorubicin and adriamycin are important clinically useful drugs in the treatment of a number of human cancers.The structurally simplified synthetic analogues 4-demethoxydaunorubicin and 4-demethoxyadriamycin show much clinical promise.The synthesis of the corresponding aglycon (+/-)-4-demethoxydaunomycinone from the inexpensive dye intermediate quinizarin, utilizing o-quinodimethane intermediates, is discussed.