CAS 128156-55-8

4-Benzoxazolecarboxylic acid, 2-methyl-, methyl ester

Description:

4-Benzoxazolecarboxylic acid, 2-methyl-, methyl ester is an organic compound characterized by its benzoxazole ring structure, which is a fused bicyclic compound containing both benzene and oxazole moieties. This compound features a carboxylic acid functional group that has been esterified with methanol, resulting in a methyl ester. The presence of the methyl group at the 2-position of the benzoxazole ring contributes to its unique chemical properties, including potential variations in solubility and reactivity compared to its non-methylated counterparts. Typically, compounds like this exhibit moderate polarity, which can influence their interactions in biological systems and their utility in various chemical applications. The compound may also display fluorescence properties, making it of interest in materials science and organic synthesis. Additionally, its structural features suggest potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards.

Formula: C₁₀H₉NO₃

InChI: InChI=1S/C10H9NO3/c1-6-11-9-7(10(12)13-2)4-3-5-8(9)14-6/h3-5H,1-2H3

InChI key: InChIKey=XDEABWGAOREBSR-UHFFFAOYSA-N

SMILES: C(OC)(=O)C1=C2C(OC(C)=N2)=CC=C1

Synonyms:

• 2-Methylbenzoxazole-4-carboxylic acid methyl ester
• 4-Benzoxazolecarboxylic acid, 2-methyl-, methyl ester
• Methyl 2-methyl-4-benzoxazolecarboxylate

Methyl 2-methylbenzo[d]oxazole-4-carboxylate

CAS: 128156-55-8

Formula: C₁₀H₉NO₃

Molecular weight: 191.1834

Ref: IN-DA00HRRL

Methyl 2-methylbenzo[D]oxazole-4-carboxylate

CAS: 128156-55-8

Methyl 2-methylbenzo[D]oxazole-4-carboxylate is a potent inhibitor of the polymerase enzyme, which plays a central role in DNA replication. It has been shown to have anticancer activity and can be used as an adjuvant therapy for cancer. The inhibitory effect of methyl 2-methylbenzo[D]oxazole-4-carboxylate on polymerase can be potentiated by other drugs such as adenosine-5'-diphosphoribose (ADP) and carboplatin. Methyl 2-methylbenzo[D]oxazole-4-carboxylate binds to the active site of polymerase through hydrogen bonding, inhibiting the synthesis of DNA. This drug also stabilizes the conformation of the enzyme's active site, which may lead to increased rates of catalysis. The reactive nature of methyl 2-methylbenzo [D] oxazole 4 car

Formula: C₁₀H₉NO₃

Purity: Min. 95%

Molecular weight: 191.18 g/mol

Ref: 3D-DFA15655