CAS 71616-84-7

Benzoic acid, 4-(4-methoxybenzoyl)-, methyl ester

Description:

Benzoic acid, 4-(4-methoxybenzoyl)-, methyl ester, also known by its CAS number 71616-84-7, is an organic compound that belongs to the class of benzoic acid derivatives. This substance features a benzoate structure with a methoxy group and a methyl ester functional group, contributing to its chemical properties. It is typically a white to off-white solid at room temperature and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water. The presence of the methoxy group enhances its lipophilicity, making it more amenable to various organic reactions. This compound may exhibit biological activity, including potential antimicrobial or antifungal properties, which can be attributed to its structural characteristics. Its applications can range from use in pharmaceuticals to agrochemicals, depending on its reactivity and functional properties. As with many organic compounds, handling should be done with care, following appropriate safety guidelines to mitigate any potential hazards.

Formula: C₁₆H₁₄O₄

InChI: InChI=1S/C16H14O4/c1-19-14-9-7-12(8-10-14)15(17)11-3-5-13(6-4-11)16(18)20-2/h3-10H,1-2H3

InChI key: InChIKey=XISRQQMWSGOFJV-UHFFFAOYSA-N

SMILES: C(=O)(C1=CC=C(C(OC)=O)C=C1)C2=CC=C(OC)C=C2

Synonyms:

• 4-(4-Methoxybenzoyl)benzoic acid methyl ester
• Benzoic Acid, 4-(4-Methoxybenzoyl)-, Methyl Ester
• NSC 86530
• Methyl 4-(4-methoxybenzoyl)benzoate
• Methyl 4-(4-Methoxybenzoyl)benzoate

4-(4-METHOXY-BENZOYL)-BENZOIC ACIDMETHYL ESTER

CAS: 71616-84-7

Formula: C₁₆H₁₄O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 270.2800

Ref: IN-DA005RG5

Methyl 4-(4-methoxybenzoyl)benzoate

CAS: 71616-84-7

Methyl 4-(4-methoxybenzoyl)benzoate

Purity: 98%

Molecular weight: 270.28g/mol

Ref: 54-OR92416

METHYL 4-(4-METHOXYBENZOYL)BENZOATE

CAS: 71616-84-7

Purity: 98%

Molecular weight: 270.2839966

Ref: 10-F845031

NSC 86530

CAS: 71616-84-7

NSC 86530 is an alkylating agent, which is a synthetic compound with the primary function of interfering with DNA replication. This compound originates from a class of chemicals known for their ability to form covalent bonds with nucleophilic sites in DNA. Its mode of action involves the formation of cross-links between DNA strands, leading to strand breakage and disrupted DNA synthesis. This interference with the DNA replication process is crucial in halting the proliferation of rapidly dividing cancer cells.

Formula: C₁₆H₁₄O₄

Purity: Min. 95%

Molecular weight: 270.28 g/mol

Ref: 3D-WCA61684