ChemicalBook--->CAS DataBase List--->6342-70-7

6342-70-7

6342-70-7 Structure

6342-70-7 Structure
IdentificationMore
[Name]

Methyl 3-methoxysalicylate
[CAS]

6342-70-7
[Synonyms]

2-HYDROXY-3-METHOXYBENZOIC ACID METHYL ESTER
AKOS 214-56
METHYL 2-HYDROXY-3-METHOXY-BENZOATE
METHYL 3-METHOXYSALICYLATE
RARECHEM AL BF 0033
[EINECS(EC#)]

228-737-5
[Molecular Formula]

C9H10O4
[MDL Number]

MFCD00239511
[Molecular Weight]

182.17
[MOL File]

6342-70-7.mol
Chemical PropertiesBack Directory
[Melting point ]

65-68 °C (lit.)
[Boiling point ]

105 °C(Press: 2 Torr)
[density ]

1.216±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

9.76±0.10(Predicted)
[color ]

White to Gray to Red
[λmax]

320nm(Dioxane)(lit.)
[InChI]

InChI=1S/C9H10O4/c1-12-7-5-3-4-6(8(7)10)9(11)13-2/h3-5,10H,1-2H3
[InChIKey]

BWRCJLJJIXYLNV-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC=CC(OC)=C1O
[CAS DataBase Reference]

6342-70-7(CAS DataBase Reference)
Safety DataBack 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 .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[HS Code ]

29189900
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3-methoxysalicylate(6342-70-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

6342-70-7(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

3-Methoxysalicylic acid

877-22-5

Methyl 3-methoxysalicylate

6342-70-7

General procedure for the synthesis of methyl 2-hydroxy-3-methoxybenzoate from methanol and 3-methoxysalicylic acid: 25.5 g (0.152 mol) of 3-methoxysalicylic acid was added to 250 ml of methanol containing 1 ml of concentrated sulfuric acid. The reaction mixture was heated to reflux for 4 days. After completion of the reaction, the mixture was concentrated to dryness. The concentrate was extracted with ethyl acetate. The organic layer was washed sequentially with water, 10% sodium carbonate solution, water and saturated sodium chloride solution. After the above treatment, 25.2 g of the target product methyl 2-hydroxy-3-methoxybenzoate was obtained in 91.2% yield. The melting point was 68-69°C.

[References]

[1] Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 9, p. 1447 - 1456
[2] Patent: KR2018/56603, 2018, A. Location in patent: Paragraph 0441; 0453-0455
[3] Australian Journal of Chemistry, 2003, vol. 56, # 11, p. 1099 - 1106
[4] Synthetic Communications, 1995, vol. 25, # 6, p. 915 - 920
[5] Journal of Medicinal Chemistry, 1991, vol. 34, # 5, p. 1612 - 1624
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