Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI)

Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI) Suppliers list
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Products Intro: Product Name:3-Methylpyrrole-2-carboxylic Acid
CAS:90724-57-5
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Products Intro: Product Name:3-Methyl-1H-pyrrole-2-carboxylic acid
CAS:90724-57-5
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Products Intro: Product Name:Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI)
CAS:90724-57-5
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CAS:90724-57-5
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Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI) manufacturers

Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI) Basic information
Product Name:Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI)
Synonyms:Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI);Pyrrole-2-carboxylic acid, 3-methyl-;3-Methylpyrrole-2-carboxylic Acid;3-Methyl-1H-pyrrole-2-carboxylicacid;3-Methyl-1H-pyrrol-2-carboxylic acid
CAS:90724-57-5
MF:C6H7NO2
MW:125.13
EINECS:
Product Categories:PYRROLE
Mol File:90724-57-5.mol
Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI) Structure
Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI) Chemical Properties
Melting point 200 °C (decomp)
Boiling point 322.4±22.0 °C(Predicted)
density 1.295±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka5.10±0.50(Predicted)
AppearanceWhite to gray Solid
Safety Information
HS Code 2933998090
MSDS Information
Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI) Usage And Synthesis
Synthesis
METHYL 3-METHYL-1H-PYRROLE-2-CARBOXYLATE

40611-69-6

Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI)

90724-57-5

General procedure for the synthesis of 3-methyl-1H-pyrrole-2-carboxylic acid from methyl 3-methyl-1H-pyrrole-2-carboxylate: 1. dissolve methyl 3-methyl-1H-pyrrole-2-carboxylate (2.0 g, 14.37 mmol, purchased from Otava Chemicals, Catalog No. 1056278) in 50 mL of methanol. 2. 21.5 mL of 2N aqueous sodium hydroxide was added to the solution. 3. The reaction mixture was stirred overnight at room temperature, then warmed to 60 °C and continued stirring for 20 hours. 4. Upon completion of the reaction, the methanol was removed by vacuum evaporation. 5. The remaining aqueous solution was neutralized with 21.5 mL of 2N hydrochloric acid solution. 6. The product was extracted using a 95:5 chloroform/methanol mixture. 7. The organic phase was washed with brine, dried over magnesium sulfate, filtered and evaporated in vacuum. 8. 1.38 g (77% yield) of the target compound 3-methyl-1H-pyrrole-2-carboxylic acid was obtained as a brown solid. LRMS (m/z): 126 (M + 1)+. 1H NMR (400 MHz, DMSO) δ 12.06 (s, 1H), 11.30 (s, 1H), 6.84-6.75 (m, 1H), 6.02-5.93 (m, 1H), 2.24 (s, 3H).

References[1] Patent: WO2012/146666, 2012, A1. Location in patent: Page/Page column 105
[2] Patent: EP2518070, 2012, A1. Location in patent: Page/Page column 44
[3] Patent: WO2014/60431, 2014, A1. Location in patent: Page/Page column 91
[4] Patent: WO2014/60432, 2014, A1. Location in patent: Page/Page column 122; 123
Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI) Preparation Products And Raw materials
Raw materialsMETHYL 3-METHYL-1H-PYRROLE-2-CARBOXYLATE-->OTAVA-BB BB7118560909-->Hydrochloric acid-->Methanol-->Water-->Sodium hydroxide
Tag:Pyrrole-2-carboxylic acid, 3-methyl- (6CI,7CI)(90724-57-5) Related Product Information
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