1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID Basic information
- Product Name:
- 1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- Synonyms:
-
- IFLAB-BB F2124-0619
- ASINEX-REAG BAS 10145669
- ART-CHEM-BB B000227
- AKOS PAO-0317
- AKOS B000227
- 1-methylpyrazole-4-carboxylic acid
- 1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- TIMTEC-BB SBB000052
- CAS:
- 5952-92-1
- MF:
- C5H6N2O2
- MW:
- 126.11
- Product Categories:
-
- Building Blocks
- C3 to C5
- Chemical Synthesis
- Heterocyclic Building Blocks
- Pyrazoles
- Mol File:
- 5952-92-1.mol
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID Chemical Properties
- Melting point:
- 203-208°C
- Boiling point:
- 306.9±15.0 °C(Predicted)
- Density
- 1.34±0.1 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- 3.88±0.10(Predicted)
- form
- Powder or Crystalline Powder
- color
- White to pale yellow
- InChI
- InChI=1S/C5H6N2O2/c1-7-3-4(2-6-7)5(8)9/h2-3H,1H3,(H,8,9)
- InChIKey
- UPPPWUOZCSMDTR-UHFFFAOYSA-N
- SMILES
- N1(C)C=C(C(O)=O)C=N1
- CAS DataBase Reference
- 5952-92-1(CAS DataBase Reference)
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID Usage And Synthesis
Uses
1-Methylpyrazol-4-carboxylic acid is an organic intermediate that can be used to prepare an amide-substituted xanthine derivative, 1-methyl-1H-pyrazol-4-carboxylic acid {4-[3-cyclopropylmethyl-1-(2-fluoro-benzyl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]-phenyl}-methyl-amide, which has gluconeogenesis-regulating activity.
Definition
ChEBI: 1-methyl-pyrazole-4-carboxylic acid is a member of the class of pyrazoles that is N-methylpyrazole substituted by a carboxy group at position 4. It has a role as a metabolite. It is a member of pyrazoles and a monocarboxylic acid. It is functionally related to a N-methylpyrazole.
Synthesis
85290-80-8
5952-92-1
General procedure for the synthesis of 1-methyl-1H-pyrazole-4-carboxylic acid from ethyl 1-methyl-1H-pyrazole-4-carboxylate: 1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (20.2 g, 131 mmol) and sodium hydroxide (6.3 g, 158 mmol) were dissolved in 200 mL of anhydrous ethanol and heated to reflux for 2 h. The stirring process was continued at room temperature for the subsequent 18 hour. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in water and the aqueous solution was washed with ether and subsequently acidified with concentrated hydrochloric acid. The precipitated solid was collected, filtered, washed with water and dried in air to give 14.2 g of 1-methyl-1H-pyrazole-4-carboxylic acid in 86% yield.
References
[1] Patent: US5498630, 1996, A
[2] Patent: US2004/14766, 2004, A1
[3] Patent: US2004/14766, 2004, A1
[4] Patent: WO2003/106459, 2003, A1. Location in patent: Page 116; 156
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materials
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACIDSupplier
- Tel
- 13915872857
- hannengchemical@163.com
- Tel
- 0516-0516-88997009 18651776937
- 4164357@qq.com
- Tel
- 025-86182925 17749516701
- 195645838@qq.com
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID(5952-92-1)Related Product Information
- 5-AMINO-4-CARBETHOXY-1-PHENYLPYRAZOLE
- ETHYL 5-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLATE
- 1-PHENYL-5-PROPYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- 5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER
- 1-METHYL-5-NITRO-1H-PYRAZOLE-4-CARBOXYLIC ACID
- ETHYL 2-PHENYL-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBOXYLATE
- 5-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- 5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID
- Ethyl 3-methyl-1H-pyrazole-5-carboxylate
- 4-BROMO-5-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID
- 5-Methyl-1H-pyrazole-3-carboxylic acid
- 4-CHLORO-1-METHYL-3-(2-METHYLPROPYL)-1H-PYRAZOLE-5-CARBOXYLIC ACID
- 4-CHLORO-3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID
- 4-CHLORO-3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER
- 4-CHLORO-1-ETHYL-3-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER
- Ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate
- 1-Methyl-1H-pyrazole-5-carboxylic acid
- 2-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL)PYRAZOLE-4-CARBOXYLIC ACID