| Identification | More | [Name]
Ethyl 3-methyl-1H-pyrazole-5-carboxylate | [CAS]
4027-57-0 | [Synonyms]
5-METHYL-2H-PYRAZOLE-3-CARBOXYLIC ACID ETHYL ESTER
AKOS PAO-0427
BUTTPARK 29\06-79
ETHYL 3-METHYL-1H-PYRAZOLE-5-CARBOXYLATE
ETHYL 3-METHYL-5-PYRAZOLECARBOXYLATE
ETHYL 3-METHYLPYRAZOLE-5-CARBOXYLATE
ETHYL 5-METHYL-2H-PYRAZOLE-3-CARBOXYLATE
1H-Pyrazole-3-carboxylic acid, 5-methyl-, ethyl ester
3-Methylpyrazole-5-carboxylic acid ethyl ester
Ethyl 3-methyl-1h-pyrazole-5-carboxylate, 95+%
Ethyl 3-methylpyrazole-5-carboxylate ,98%
5-Methyl-1H-pyrazole-3-carboxylic acid ethyl ester | [EINECS(EC#)]
223-702-0 | [Molecular Formula]
C7H10N2O2 | [MDL Number]
MFCD00052514 | [Molecular Weight]
154.17 | [MOL File]
4027-57-0.mol |
| Chemical Properties | Back Directory | [Melting point ]
80-84 °C (lit.) | [Boiling point ]
299.1±20.0 °C(Predicted) | [density ]
1.171±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
powder to crystal | [pka]
11.60±0.10(Predicted) | [color ]
White to Light yellow | [Detection Methods]
HPLC | [BRN ]
4192 | [InChI]
InChI=1S/C7H10N2O2/c1-3-11-7(10)6-4-5(2)8-9-6/h4H,3H2,1-2H3,(H,8,9) | [InChIKey]
BOTXQJAHRCGJEG-UHFFFAOYSA-N | [SMILES]
N1C(C)=CC(C(OCC)=O)=N1 | [CAS DataBase Reference]
4027-57-0(CAS DataBase Reference) | [NIST Chemistry Reference]
3(5)-methyl-5(3)-ethoxycarbonylpyrazole(4027-57-0) | [Storage Precautions]
Moisture sensitive |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29331990 |
| Hazard Information | Back Directory | [Chemical Properties]
White to yellow solid | [Uses]
Ethyl 3-Methyl-5-pyrazolecarboxylate is a useful synthetic intermediate. It is used to prepare tetrahydroisoquinoline amide substituted Ph pyrazoles as selective Bcl-2 inhibitors. It is also studies as a hypolipidemic agent. | [General Description]
Ethyl 3-methylpyrazole-5-carboxylate can be prepared by reacting ethyl acetylpyruvate and hydrazine. |
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