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540234

Sigma-Aldrich

Dimethyl 2,5-pyridine dicarboxylate

97%

Synonym(s):

Methyl 6-methoxycarbonyl nicotinate

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About This Item

Empirical Formula (Hill Notation):
C9H9NO4
CAS Number:
881-86-7
Molecular Weight:
195.17
MDL number:
MFCD00034767
UNSPSC Code:
12352100
PubChem Substance ID:
24878448
NACRES:
NA.22

assay

97%

mp

213-217 °C (lit.)

SMILES string

COC(=O)c1ccc(nc1)C(=O)OC

InChI

1S/C9H9NO4/c1-13-8(11)6-3-4-7(10-5-6)9(12)14-2/h3-5H,1-2H3

InChI key

TUGSJNQAIMFEDY-UHFFFAOYSA-N

Related Categories

General description

Dimethyl 2,5-pyridine dicarboxylate can be prepared from 2,5-pyridinedicarboxylic acid.

Application

Dimethyl 2,5-pyridine dicarboxylate (Dimethyl 2,5-pyridinedicarboxylate) may be used in the synthesis of:
  • 2,5-dicarbomethoxy-N-methylpyridinium methosulfate
  • 2,5-dicarboxy-N-methylpyridinium betaine
  • 6-carbomethoxy-2-carboxypyridine-N-oxide

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Nitrogen-Substituted Derivatives of 2, 5-Pyridinedicarboxylic Acid.
Peterson ML.
The Journal of Organic Chemistry, 25(4), 565-569 (1960)
Marta Soler et al.
Inorganic chemistry, 54(22), 10542-10558 (2015-10-28)
The conjugation of redox-active complexes that can function as chemical nucleases to cationic tetrapeptides is pursued in this work in order to explore the expected synergistic effect between these two elements in DNA oxidative cleavage. Coordination complexes of biologically relevant

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