| Identification | More | [Name]
Methyl 4-methoxysalicylate | [CAS]
5446-02-6 | [Synonyms]
2-HYDROXY-4-METHOXY-BENZOIC ACID METHYL ESTER
4-METHOXYSALICYLIC ACID METHYL ESTER
ASISCHEM Z67646
METHYL 2-HYDROXY-4-METHOXYBENZOATE
METHYL 4-METHOXYSALICYLATE
RARECHEM AL BF 0038
Benzoic acid, 2-hydroxy-4-methoxy-, methyl ester
2-Hydroxy-4-methoxybenzoic acid methyl ester~Methyl 4-methoxysalicylate
Methyl P-Methoxysalicylate
MethylP-Methoxysalicylate(2-Hydroxy-4-MethoxybenzoicAcidMethylEster)
methyl 2-hydroxy-p-anisate
Methyl 2-hydroxy-4-methoxybenzoate 98%
methyl 2-hydroxy-4-methoxybenzoic acid
4-Methoxysalicylic Acid Methyl
Methyl-2 hydroxy-4-4-Methoxybenzoate | [EINECS(EC#)]
226-657-5 | [Molecular Formula]
C9H10O4 | [MDL Number]
MFCD00008424 | [Molecular Weight]
182.17 | [MOL File]
5446-02-6.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystalline powder | [Melting point ]
50-53 °C (lit.) | [Boiling point ]
134°C 7mm | [density ]
1.1634 (rough estimate) | [refractive index ]
1.4600 (estimate) | [Fp ]
>230 °F
| [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Crystalline Powder or Crystals | [color ]
White to light yellow | [Water Solubility ]
Soluble in acetone. Insoluble in water. | [BRN ]
2691644 | [InChIKey]
ZICRWXFGZCVTBZ-UHFFFAOYSA-N | [LogP]
2.430 (est) | [CAS DataBase Reference]
5446-02-6(CAS DataBase Reference) | [NIST Chemistry Reference]
Methyl 4-methoxysalicylate(5446-02-6) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HS Code ]
29189900 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystalline powder | [Uses]
Methyl 4-methoxysalicylate (methyl 2-hydroxy-4-methoxybenzoate) was used in the enantioselective synthesis of (+)-coriandrone A and B, two bioactive natural products. |
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