| Identification | More | [Name]
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID | [CAS]
5952-92-1 | [Synonyms]
1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
AKOS B000227
AKOS PAO-0317
ART-CHEM-BB B000227
ASINEX-REAG BAS 10145669
IFLAB-BB F2124-0619
TIMTEC-BB SBB000052
1-methyl-4-pyrazolecarboxylic acid | [Molecular Formula]
C5H6N2O2 | [MDL Number]
MFCD00159641 | [Molecular Weight]
126.11 | [MOL File]
5952-92-1.mol |
| Chemical Properties | Back Directory | [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 | [form ]
Powder or Crystalline Powder | [pka]
3.88±0.10(Predicted) | [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) |
| Questions And Answer | Back Directory | [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. |
| Hazard Information | Back Directory | [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]
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 |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|