W271705

Methyl 2-methoxybenzoate

≥97%

• Sinônimo(s): Methyl o-anisate
• Fórmula linear: CH₃OC₆H₄CO₂CH₃
• Número CAS: 606-45-1
• Peso molecular: 166.17
• Número FEMA: 2717
• Número CE: 210-118-6
• Conselho da Europa nº: 2192
• Número MDL: MFCD00008423
• Código UNSPSC: 12164502
• ID de substância PubChem: 24901281
• Número de Flavis: 9.796
• NACRES: NA.21

Propriedades

• fonte biológica: synthetic
• Nível de qualidade: 400
• grau: Kosher
• Agency: meets purity specifications of JECFA
• Ensaio: ≥97%
• índice de refração: n20/D 1.534 (lit.)
• p.e.: 248 °C (lit.)
• densidade: 1.157 g/mL at 25 °C (lit.)
• aplicação(ões): flavors and fragrances
• Documentação: see Safety & Documentation for available documents
• alérgeno alimentar: no known allergens
• Organoléptico: hyacinth; herbaceous
• cadeia de caracteres SMILES: COC(=O)c1ccccc1OC
• InChI: 1S/C9H10O3/c1-11-8-6-4-3-5-7(8)9(10)12-2/h3-6H,1-2H3
• chave InChI: PFYHAAAQPNMZHO-UHFFFAOYSA-N

Descrição

Aplicação

• Characterizing Repellencies of Methyl Benzoate and Its Analogs against the Common Bed Bug, Cimex lectularius.: This study evaluates the repellent effects of Methyl 2-methoxybenzoate among other methyl benzoate analogs against bed bugs, highlighting its potential in developing non-toxic pest control solutions (Strickland et al., 2022).


• Copper-catalysed intramolecular O-arylation: a simple and efficient method for benzoxazole synthesis.: This research uses Methyl 2-methoxybenzoate as a ligand in the synthesis of benzoxazole, a compound with significant pharmaceutical applications, via copper-catalyzed reactions (Wu et al., 2014).


• Attraction of the orange mint moth and false celery leaftier moth (Lepidoptera: Crambidae) to floral chemical lures.: Explores the use of Methyl 2-methoxybenzoate in agricultural pest management, specifically its role in attracting and managing pest populations in crop fields (Landolt et al., 2014).


• Synthesis of (+/-)- and (-)-vibralactone and vibralactone C.: Discusses the synthetic applications of Methyl 2-methoxybenzoate in creating complex organic molecules, such as vibralactone, which are important in medicinal chemistry and biological research (Zhou and Snider, 2008).

Exoneração de responsabilidade

For R&D or non-EU Food use. Not for retail sale.

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 2
• Ponto de fulgor (°F): 235.4 °F - closed cup
• Ponto de fulgor (°C): 113 °C - closed cup
• Equipamento de proteção individual: dust mask type N95 (US), Eyeshields, Gloves