| Identification | Back Directory | [Name]
Methyl 3-hydroxy-4-methoxybenzoate | [CAS]
6702-50-7 | [Synonyms]
METHYL ISOVANILLATE
RARECHEM AL BF 0068
Methyl 3-hydroxy-4-m
METHYL 3-HYDROXY-4-METHOXYBENZOATE
Methyl 3-hydroxy-4-methoxybenzoate,98%
Methyl 3-hydroxy-4-methoxybenzoate 98%
METHYL 3-HYDROXY-4-METHOXYBENZENECARBOXYLATE
3-Hydroxy-4-Methoxy-benzoic acid Methyl ester
3 - hydroxy - 4 - Methoxy Methyl benzoic acid
benzoic acid, 3-hydroxy-4-methoxy-, methyl ester
Methyl 3-hydroxy-4-methoxybenzoateMethyl isovanillate
2-Methoxy-5-(methoxycarbonyl)phenol, 2-Hydroxy-4-(methoxycarbonyl)anisole, Methyl isovanillate | [Molecular Formula]
C9H10O4 | [MDL Number]
MFCD01321262 | [MOL File]
6702-50-7.mol | [Molecular Weight]
182.17 |
| Chemical Properties | Back Directory | [Appearance]
Off-white to beige crystalline powder | [Melting point ]
64-67 °C(lit.)
| [Boiling point ]
102 °C(Press: 0.1 Torr) | [density ]
1.216±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
powder to crystal | [pka]
9.15±0.10(Predicted) | [color ]
Light yellow to Brown | [LogP]
1.750 (est) |
| Hazard Information | Back Directory | [Chemical Properties]
Off-white to beige crystalline powder | [Uses]
Methyl 3-hydroxy-4-methoxybenzoate may be used as starting reagent in the novel synthesis of gefitinib. Synthesis involves the alkylation of starting material, followed by nitration, reduction, cyclization, chlorination and two successive amination reactions. It may be used as starting reagent in the synthesis of methyl 5-(benzo[d][1,3]dioxol-5-yl)-4-methoxy-2-nitrobenzoate. |
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