CAS 7598-10-9

2-bromomethyl-anthraquinone

Description:

2-Bromomethyl-anthraquinone is an organic compound characterized by its anthraquinone structure, which consists of a three-ring system with two carbonyl groups. The presence of a bromomethyl group at the 2-position of the anthraquinone framework introduces both halogen and alkyl functionalities, influencing its reactivity and solubility. This compound typically appears as a solid and is known for its vibrant color, which is common among anthraquinone derivatives. It is often utilized in dye chemistry and as an intermediate in organic synthesis due to its ability to undergo various chemical transformations, including electrophilic substitution and nucleophilic addition reactions. Additionally, 2-bromomethyl-anthraquinone may exhibit biological activity, making it of interest in medicinal chemistry. Its properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and purity of the sample. Safety precautions should be taken when handling this compound, as it may pose health risks associated with halogenated organic compounds.

Formula: C₁₅H₉BrO₂

InChI: InChI=1/C15H9BrO2/c16-8-9-5-6-12-13(7-9)15(18)11-4-2-1-3-10(11)14(12)17/h1-7H,8H2

InChI key: FCETXLHFBYOVCV-UHFFFAOYSA-N

SMILES: c1ccc2c(c1)C(=O)c1ccc(cc1C2=O)CBr

Synonyms:

• 2-(Bromomethyl)Anthracene-9,10-Dione
• 2-(Bromomethyl)Anthraquinone

2-(Bromomethyl)Anthracene-9,10-Dione

CAS: 7598-10-9

2-(Bromomethyl)Anthracene-9,10-Dione

Formula: C₁₅H₉BrO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 301.13

Ref: 54-OR1027658

2-Bromomethyl-anthraquinone

CAS: 7598-10-9

Formula: C₁₅H₉BrO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 301.1348

Ref: IN-DA003GS4

2-Bromomethyl-anthraquinone

CAS: 7598-10-9

Purity: 97%;RG

Molecular weight: 301.1390076

Ref: 10-F866069

2-Bromomethyl anthraquinone

CAS: 7598-10-9

2-Bromomethyl anthraquinone (2BMAA) is a non-steroidal anti-inflammatory drug that has been shown to inhibit the growth of cancer cells in vitro. It has been shown to inhibit tumor cell growth by inhibiting fatty acid synthesis and by binding to fatty acid receptors on the surface of tumor cells. 2BMAA also inhibits cancer cell proliferation by preventing the transfer of electrons from cytochrome c oxidase to oxygen, preventing the formation of superoxide anions, and suppressing lipid peroxidation. The photophysical properties of 2BMAA have been studied using cyclic voltammetry and electrochemical studies. 2BMAA is a potent inhibitor of bladder cancer in mice, with a diameter inhibition ranging from 40% at 10 µM to 100% at 70 µM. It has also been shown to be effective against other cancers such as prostate, breast, lung and skin cancers. This compound is synthesized on a solid phase through the use of electro

Formula: C₁₅H₉BrO₂

Purity: Min. 95%

Molecular weight: 301.13 g/mol

Ref: 3D-FB49812