CAS 869-09-0

Pentanedioic acid, 2,4-dibromo-, dimethyl ester

Description:

Pentanedioic acid, 2,4-dibromo-, dimethyl ester, commonly known as dimethyl 2,4-dibromoadipate, is an organic compound characterized by its structure, which includes a five-carbon dicarboxylic acid backbone with two bromine substituents at the 2 and 4 positions and two methyl ester groups. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water due to its hydrophobic alkyl chains. The presence of bromine atoms enhances its reactivity, making it useful in various chemical synthesis applications, including the production of pharmaceuticals and agrochemicals. Additionally, the compound exhibits properties typical of esters, such as pleasant odors and the ability to undergo hydrolysis in the presence of water or acids. Safety considerations include handling it with care due to potential toxicity and environmental impact, as brominated compounds can pose risks to aquatic life.

Formula: C₇H₁₀Br₂O₄

Synonyms:

• 1,5-dimethyl 2,4-dibromopentanedioate
• 2,4-Dibromo-Pentanedioic Acid Dimethyl Ester
• Dimethyl 2,4-dibromopentanedioate

Pentanedioic acid, 2,4-dibromo-, dimethyl ester

CAS: 869-09-0

Formula: C₇H₁₀Br₂O₄

Purity: 98%

Color and Shape: Liquid

Molecular weight: 317.9599

Ref: IN-DA008EI3

Dimethyl 2,4-dibromopentanedioate

CAS: 869-09-0

Dimethyl 2,4-dibromopentanedioate

Purity: 95%

Molecular weight: 317.96g/mol

Ref: 54-OR1070664

Dimethyl 2,4-dibromoglutarate

CAS: 869-09-0

Formula: C₇H₁₀Br₂O₄

Purity: 95%

Molecular weight: 317.961

Ref: 10-F050904

Dimethyl 2,4-dibromoglutarate

CAS: 869-09-0

Dimethyl 2,4-dibromoglutarate is a stereospecific, unselective opioid receptor ligand. It interacts with the opioid receptors and has been shown to have affinity for both mu and kappa receptors. Dimethyl 2,4-dibromoglutarate has been studied as a potential model for morphine and other selective ligands. The two enantiomers of dimethyl 2,4-dibromoglutarate were synthesized in order to study their selectivity for the opioid receptor. The racemic mixture of dimethyl 2,4-dibromoglutarate was found to be more potent than either of the individual enantiomers. The cyclopropane ring on the left side of the molecule is responsible for this effect. This ring confers higher affinity and selectivity than that on the right side of the molecule.

Formula: C₇H₁₀Br₂O₄

Purity: Min. 95%

Molecular weight: 317.96 g/mol

Ref: 3D-AAA86909