ChemicalBook--->CAS DataBase List--->4670-56-8

4670-56-8

4670-56-8 Structure

4670-56-8 Structure
IdentificationMore
[Name]

Methyl 4-methylsalicylate
[CAS]

4670-56-8
[Synonyms]

2-HYDROXY-4-METHYLBENZOIC ACID METHYL ESTER
4-METHYLSALICYLIC ACID METHYL ESTER
METHYL 2-HYDROXY-4-METHYLBENZOATE
METHYL 4-METHYLSALICYLATE
METHYL M-CRESOTATE
METHYL M-CRESOTINATE
RARECHEM AL BF 0822
TIMTEC-BB SBB008512
2-hydroxy-4-methyl-benzoicacimethylester
Benzoicacid,2-hydroxy-4-methyl-,methylester
Methyl4-Methylsalicylate(2-Hydroxy-4-MethybenzoicAcidMethylEster)
Methyl-4-Methyl
METHYL-4-MEHTYL SALICYLATE
[EINECS(EC#)]

225-117-6
[Molecular Formula]

C9H10O3
[MDL Number]

MFCD00020130
[Molecular Weight]

166.17
[MOL File]

4670-56-8.mol
Chemical PropertiesBack Directory
[Melting point ]

27-28℃
[Boiling point ]

242 °C
[density ]

1.147
[Fp ]

28 °C
[refractive index ]

1.5370
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

Low Melting Solid
[pka]

9.87±0.10(Predicted)
[color ]

Pale brown to pale yellow
[FreezingPoint ]

24.0 to 28.0 ℃
[Cosmetics Ingredients Functions]

PERFUMING
[InChI]

InChI=1S/C9H10O3/c1-6-3-4-7(8(10)5-6)9(11)12-2/h3-5,10H,1-2H3
[InChIKey]

UITFCFWKYAOJEJ-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC=C(C)C=C1O
[LogP]

3.000 (est)
[CAS DataBase Reference]

4670-56-8(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[REACH Registrations]

Active
[HS Code ]

2918230000
Hazard InformationBack Directory
[Synthesis Reference(s)]

Journal of the American Chemical Society, 102, p. 3534, 1980 DOI: 10.1021/ja00530a038
[Synthesis]

3-Hydroxy-4-methylbenzoic acid

586-30-1

Methyl 4-methylsalicylate

4670-56-8

Step 1: 3-hydroxy-4-methylbenzoic acid (4.56 g, 30 mmol) was dissolved in methanol (60 mL) and thionyl chloride (40 drops) was added slowly and dropwise. The reaction mixture was heated to reflux and maintained for 18 hours. Upon completion of the reaction, the volatile components were removed by distillation under reduced pressure. The crude product was purified by fast column chromatography on silica gel, using gradient elution with ethyl acetate/heptane (2%-40%) to afford methyl 2-hydroxy-4-methylbenzoate (3.04 g, 61% yield) as a colorless oil. Mass spectrometry analysis (ESI/APCI+): m/z 167 ([M-H]-).

[References]

[1] Patent: WO2010/130842, 2010, A1. Location in patent: Page/Page column 132-133
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 4-methylsalicylate(4670-56-8)1HNMR
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

Methyl 4-Methylsalicylate,>98.0%(GC)(4670-56-8)
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