ChemicalBook--->CAS DataBase List--->81452-54-2

81452-54-2

81452-54-2 Structure

81452-54-2 Structure
IdentificationBack Directory
[Name]

METHYL 3-METHYLTHIOPHENE-2-CARBOXYLATE
[CAS]

81452-54-2
[Synonyms]

RARECHEM AL BF 0178
3-Methylthiophene-2-Cabroxylate
3-methylthiophene-2-carboxylate
Eethyl3-methylthiophene-2-carboxylate
METHYL 3-METHYLTHIOPHENE-2-CARBOXYLATE
Methyl 3-Methylthiophene-2-carboxylate >
Methyl 3-methylthiophene-2-carboxylate ,99%
3-Methylthiophene-2-carboxylic acid methyl ester
3-methyl-2-thiophenecarboxylic acid methyl ester
2-Thiophenecarboxylic acid, 3-methyl-, methyl ester
METHYL 3-METHYLTHIOPHENE-2-CARBOXYLATE ISO 9001:2015 REACH
[Molecular Formula]

C7H8O2S
[MDL Number]

MFCD00234332
[MOL File]

81452-54-2.mol
[Molecular Weight]

156.2
Chemical PropertiesBack Directory
[Boiling point ]

216-217°C
[density ]

1.173±0.06 g/cm3(Predicted)
[refractive index ]

1.5168
[Fp ]

216-217°C
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Light yellow
[BRN ]

116836
[InChI]

InChI=1S/C7H8O2S/c1-5-3-4-10-6(5)7(8)9-2/h3-4H,1-2H3
[InChIKey]

BRWROFVPMUPMJQ-UHFFFAOYSA-N
[SMILES]

C1(C(OC)=O)SC=CC=1C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H227
[Precautionary statements ]

P210-P280-P403+P235-P501
[Safety Statements ]

23-24/25
[HS Code ]

29151300
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methanol-->Sulfuric acid-->Acetone-->Chromium(VI) oxide-->3-Methyl-2-thiophenecarboxaldehyde-->2-Bromo-3-methylthiophene-->Sodium bicarbonate-->3-Methyl-2-thiophenecarboxylic acid-->3-Methylthiophene-2-carbonyl chloride-->Dimethyl sulfate
[Preparation Products]

2-bromo-4H-thieno[2,3-c]pyrrol-6(5H)-one
Hazard InformationBack Directory
[Chemical Properties]

Colorless liquid
[Synthesis]

Methanol

67-56-1

3-Methyl-2-thiophenecarboxylic acid

23806-24-8

METHYL 3-METHYLTHIOPHENE-2-CARBOXYLATE

81452-54-2

Step 1: Synthesis of methyl 3-methylthiophene-2-carboxylate: 3-methylthiophene-2-carboxylic acid (15 g, 105 mmol, 1.0 eq.) was dissolved in methanol (150 mL) and concentrated sulfuric acid (7.5 mL) was added slowly and dropwise. The reaction mixture was heated to reflux for 12 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate (200 mL) and washed sequentially with water (2 x 50 mL), saturated aqueous sodium bicarbonate solution (2 x 50 mL) and brine (50 mL). The organic phase was dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to afford 20 g (97% yield) of methyl 3-methylthiophene-2-carboxylate as an oil. The product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.38 (d, J=5.0 Hz, 1H), 6.91 (d, J=5.0 Hz, 1H), 3.85 (s, 3H), 2.55 (s, 3H); ESI-MS m/z 157 ([M+H]+).

[References]

[1] Patent: WO2012/56478, 2012, A1. Location in patent: Page/Page column 75-76
[2] Patent: WO2007/124546, 2007, A1. Location in patent: Page/Page column 58
[3] Patent: WO2014/64131, 2014, A2. Location in patent: Page/Page column 114; 115
[4] Patent: WO2014/76104, 2014, A1. Location in patent: Page/Page column 79-80
[5] Journal of Medicinal Chemistry, 1995, vol. 38, # 24, p. 4806 - 4820
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 3-METHYLTHIOPHENE-2-CARBOXYLATE(81452-54-2)1HNMR
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