CAS 89555-39-5

2-Naphthalenecarboxylic acid, 1-bromo-, methyl ester

Description:

2-Naphthalenecarboxylic acid, 1-bromo-, methyl ester, with the CAS number 89555-39-5, is an organic compound characterized by its naphthalene structure, which consists of two fused benzene rings. This compound features a carboxylic acid group that is esterified with a methyl group, as well as a bromine atom attached to the first position of the naphthalene ring. The presence of the bromine substituent can influence the compound's reactivity and polarity, making it useful in various chemical reactions, such as nucleophilic substitutions. The methyl ester functional group contributes to its solubility in organic solvents and can facilitate further chemical transformations. Typically, compounds like this exhibit moderate to high melting and boiling points due to their aromatic nature and molecular interactions. Additionally, they may show biological activity, making them of interest in medicinal chemistry and material science. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

Formula: C₁₂H₉BrO₂

Synonyms:

• 1-Bromo-2-naphthoic acid methyl ester

2-Naphthalenecarboxylic Acid, 1-Bromo-, Methyl Ester

CAS: 89555-39-5

2-Naphthalenecarboxylic Acid, 1-Bromo-, Methyl Ester

Formula: C₁₂H₉BrO₂

Purity: >98%

Molecular weight: 265.1

Ref: 54-OR1010565

2-Naphthalenecarboxylic acid, 1-broMo-, Methyl ester

CAS: 89555-39-5

Formula: C₁₂H₉BrO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 265.1027

Ref: IN-DA003ZG6

Methyl 1-bromo-2-naphthoate

CAS: 89555-39-5

Methyl 1-bromo-2-naphthoate

Formula: C₁₂H₉BrO₂

Purity: 98%

Molecular weight: 265.1

Ref: IN-DG01099002

Methyl 1-bromo-2-naphthoate

CAS: 89555-39-5

Purity: 98%

Color and Shape: Solid

Molecular weight: 265.1059875

Ref: 10-F719702

2-Naphthalenecarboxylic acid, 1-bromo-, methyl ester

CAS: 89555-39-5

2-Naphthalenecarboxylic acid, 1-bromo-, methyl ester is a chiral molecule with two enantiomers. It can be synthesized from naphthalene and bromoacetic acid derivatives by an asymmetric synthesis. The diacid can be obtained through the cross-coupling of the corresponding organometallic reagent with a suitable halide. The 2-naphthacarboxylic acid, 1-bromo-, methyl ester has been used to synthesize various ligands with interesting properties. It has also been used in osmium chemistry and in enantioselective hydrogenation reactions.

Formula: C₁₂H₉BrO₂

Purity: Min. 95%

Molecular weight: 265.1 g/mol

Ref: 3D-PDA55539