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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

Quality Level

100

Assay

98%

mp

80-84 °C (lit.)

functional group

ester

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV8085
MKCJ8615
MKBK1136V
MKBF6221V
MKBC8367

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A new ester substituted heteroscorpionate ligand.
Alidori S, et al.
Inorganic Chemistry Communications, 7(9), 1075-1077 (2004)
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)

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