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558354

Sigma-Aldrich

Ethyl 3-methylpyrazole-5-carboxylate

98%

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About This Item

Empirical Formula (Hill Notation):
C7H10N2O2
CAS Number:
4027-57-0
Molecular Weight:
154.17
EC Number:
223-702-0
MDL number:
MFCD00052514
UNSPSC Code:
12352100
PubChem Substance ID:
24879738
NACRES:
NA.22

Assay

98%

mp

80-84 °C (lit.)

SMILES string

CCOC(=O)c1cc(C)n[nH]1

InChI

1S/C7H10N2O2/c1-3-11-7(10)6-4-5(2)8-9-6/h4H,3H2,1-2H3,(H,8,9)

InChI key

BOTXQJAHRCGJEG-UHFFFAOYSA-N

General description

Ethyl 3-methylpyrazole-5-carboxylate can be prepared by reacting ethyl acetylpyruvate and hydrazine.

Application

Ethyl 3-methylpyrazole-5-carboxylate may be used to synthesize the following ligands:
  • potassium salt of new dihydrobis(3-carboxyethyl-5-methylpyrazolyl)borate (BpCOOEt,Me)
  • [(3-carboxy-5-methyl-1H-1-pyrazolyl) (3-methyl-5-carboxy-1H-1-pyrazolyl)methane, which readily forms Zn(II) and Cd(II) complexes
  • bis(3-carboxy-5-methyl-1H-1-pyrazolyl)methane, which readily forms Zn(II) and Cd(II) complexes

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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29. Sulphanilamides of some aminopyrazoles, and a note on the application of p-phthalimidobenzenesulphonyl chloride to the synthesis of sulphanilamides.
Dewar MJS and King FE.
Journal of the Chemical Society, 114-116 (1945)
New N, N, O, O-functionalized heteroscorpionate ligands and related Zn (II) and Cd (II) derivatives.
Santini C.
Inorganic Chemistry Communications, 7(7), 834-837 (2004)
A new ester substituted heteroscorpionate ligand.
Alidori S, et al.
Inorganic Chemistry Communications, 7(9), 1075-1077 (2004)

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