Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate

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Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:Methyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate
CAS:110860-60-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-62967
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Products Intro: Product Name:Methyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate
CAS:110860-60-1
Purity:98% Package:$9.9/50mg;$15.9/100mg;$20.9/250mg;$25.9/1g;$71.9/5g;$128.9/10g;Bulk package Remarks:98%
Company Name: Amadis Chemical Company Limited
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Products Intro: Product Name:5-amino-1-methyl-4-pyrazolecarboxylic acid methyl ester
CAS:110860-60-1
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Company Name: Nanjing Chalf-Pharm Technology Co., Ltd.  
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Products Intro: Product Name:Methyl5-aMino-1-Methyl-1H-pyrazole-4-carboxylate
CAS:110860-60-1
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Products Intro: Product Name:5-Amino-1-methyl-1H-pyrazole-4-carboxylic acid methyl ester
CAS:110860-60-1
Purity:95% Package:1g;5g;10g;25g Remarks:B1-8555
Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate Basic information
Product Name:Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate
Synonyms:Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate;5-amino-1-methyl-4-pyrazolecarboxylic acid methyl ester;1H-Pyrazole-4-carboxylic acid, 5-amino-1-methyl-, methyl ester;methyl 5-amino-1-methylpyrazole-4-carboxylate
CAS:110860-60-1
MF:C6H9N3O2
MW:155.15
EINECS:
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Mol File:110860-60-1.mol
Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate Structure
Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate Usage And Synthesis
Synthesis
Methyl Methoxymethylenecyanoacetate

13974-74-8

Methylhydrazine

60-34-4

Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate

110860-60-1

General procedure for the synthesis of methyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate from the compound (CAS:13974-74-8) and methylhydrazine: 150 mL of isopropanol was added to 7.4 mL (141 mmol) of methylhydrazine and the resulting mixture was cooled to 15°C (internal temperature). To the cooled mixture was slowly added 7.0 g (49.6 mmol) of intermediate (a), followed by heating the reaction mixture to 50°C and stirring for 1 hour and 40 minutes. Upon completion of the reaction, the reaction solution was concentrated under reduced pressure and then the concentrate was purified by silica gel column chromatography to give 10.5 g (white powder; yield: 50%) of intermediate (b). The NMR data of the obtained intermediate (b) were as follows: 1H-NMR (300 MHz, CDCl3): δ 7.60 (s, 1H), 4.95 (brs, 2H), 3.80 (s, 3H), 3.60 (s, 3H).

References[1] Patent: WO2009/110643, 2009, A1. Location in patent: Page/Page column 100
[2] Patent: WO2010/104210, 2010, A1. Location in patent: Page/Page column 36-38
[3] Patent: EP2230278, 2010, A2. Location in patent: Page/Page column 33
[4] Patent: EP2228409, 2010, A2. Location in patent: Page/Page column 30
[5] Patent: US2011/17099, 2011, A1. Location in patent: Page/Page column 12
Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate Preparation Products And Raw materials
Raw materialsMethyl Methoxymethylenecyanoacetate-->Methylhydrazine-->2-Propenoic acid, 3-amino-2-cyano-, methyl ester
Tag:Methyl 5-aMino-1-Methyl-1H-pyrazole-4-carboxylate(110860-60-1) Related Product Information
1H-Pyrazole-4-carboxylicacid,5-amino-1-methyl-(9CI) ETHYL 5-AMINO-1-METHYLPYRAZOLE-4-CARBOXYLATE PYRAZOLE-4-CARBOXYLIC ACID, 3-AMINO-1-METHYL-, ETHYL ESTER methyl 5-amino-1,3-dimethyl-1H-pyrazole-4-carboxylate 5-Amino-1-methyl-1H-pyrazole-4-carbaldehyde 1H-Pyrazole-4-carboxylic acid, 3-aMino-1-Methyl-, Methyl ester