Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
Ethyl 1H-pyrazole-4-carboxylate, 98%, Thermo Scientific Chemicals
Have Questions?
Change view
Catalog number B25351.14
also known as B25351-14
Price (USD)/ Each
534.65
Online exclusive
594.00 Save 59.35 (10%)
-
Quantity:
25 g
Price (USD)/ Each
534.65
Online exclusive
594.00 Save 59.35 (10%)
Ethyl 1H-pyrazole-4-carboxylate, 98%, Thermo Scientific Chemicals
Catalog numberB25351.14
Price (USD)/ Each
534.65
Online exclusive
594.00 Save 59.35 (10%)
-
Chemical Identifiers
CAS37622-90-5
IUPAC Nameethyl 1H-pyrazole-4-carboxylate
Molecular FormulaC6H8N2O2
InChI KeyKACZQOKEFKFNDB-UHFFFAOYSA-N
SMILESCCOC(=O)C1=CNN=C1
View more
Specifications
Specification Sheet
Specification SheetAssay (GC)≥97.5%
Appearance (Color)White to pale yellow or pale cream
FormCrystals or powder or crystalline powder
Melting Point (clear melt)74.5-80.5?C
Ethyl 1H-pyrazole-4-carboxylate is used in the preparation of isoxazole-4-carboxylic acid derivatives and isoxazole-3,5-dicarboxamides. Further, it acts as an intermediate in organic synthesis.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Ethyl 1H-pyrazole-4-carboxylate is used in the preparation of isoxazole-4-carboxylic acid derivatives and isoxazole-3,5-dicarboxamides. Further, it acts as an intermediate in organic synthesis.
Solubility
Miscible with acetone.
Notes
Incompatible with strong oxidizing agents, strong acids and bases.
Ethyl 1H-pyrazole-4-carboxylate is used in the preparation of isoxazole-4-carboxylic acid derivatives and isoxazole-3,5-dicarboxamides. Further, it acts as an intermediate in organic synthesis.
Solubility
Miscible with acetone.
Notes
Incompatible with strong oxidizing agents, strong acids and bases.
RUO – Research Use Only
General References:
- Zheng, K.; Iqbal, S.; Hernandez, P.; Park, H.; LoGrasso, P. V.; Feng, Y. Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives. J. Med. Chem. 2014, 57 (23), 10013-10030.
- Mane, R. S.; Sasaki, T.; Bhanage, B. M. Silica supported palladium-phosphine as a reusable catalyst for alkoxycarbonylation and aminocarbonylation of aryl and heteroaryl iodides. RSC Adv. 2015, 5 (115), 94776-94785.