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I17508

Sigma-Aldrich

Isonicotinic acid

99%

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Synonym(s):
4-Picolinic acid, Pyridine-4-carboxylic acid
Empirical Formula (Hill Notation):
C6H5NO2
CAS Number:
Molecular Weight:
123.11
Beilstein/REAXYS Number:
109599
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

powder

technique(s)

cell culture | plant: suitable

mp

≥300 °C (lit.)

SMILES string

OC(=O)c1ccncc1

InChI

1S/C6H5NO2/c8-6(9)5-1-3-7-4-2-5/h1-4H,(H,8,9)

Inchi Key

TWBYWOBDOCUKOW-UHFFFAOYSA-N

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1 of 4

This Item
I17451P4280079838
vibrant-m

I17508

Isonicotinic acid

vibrant-m

I17451

Isonicotinamide

vibrant-m

P42800

2-Picolinic acid

vibrant-m

79838

Nicotinic acid

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

300

form

powder

form

-

form

crystals

form

powder

mp

≥300 °C (lit.)

mp

155-157 °C (lit.)

mp

139-142 °C (lit.)

mp

236-239 °C (lit.)

technique(s)

cell culture | plant: suitable

technique(s)

-

technique(s)

-

technique(s)

gas chromatography (GC): suitable

application

Isonicotinic acid (IN) can be used as:
  • An organocatalyst in the one pot four component condensation reaction, to synthesize pyranopyrazoles based heterocyclic compounds.
  • An organic ligand for the preparation of copper(I) halide coordination polymer [CuBr(IN)]n, by hydrothermal method.
  • As a starting material for the synthesis of cation-dimers with potent antimalarial activity.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

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


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Antimalarial Cation-dimers Synthesized in Two Steps from an Inexpensive Starting Material, Isonicotinic Acid
Motoshima K, et al.
ChemMedChem, 2(10), 1527-1532 (2007)
Hydrothermal synthesis and characterization of a copper (I) halide coordination polymer with isonicotinic acid (IN) ligand as a template possessing three-dimensional supramolecular network structure
Yu J-H, et al.
Inorganic Chemistry Communications, 5(8), 572-576 (2002)
Synthesis of pyranopyrazoles using isonicotinic acid as a dual and biological organocatalyst
Zolfigol MA, et al.
Royal Society of Chemistry Advances, 3(48), 25681-25685 (2013)
Rie Makiura et al.
Dalton transactions (Cambridge, England : 2003), 44(34), 15279-15285 (2015-06-03)
Surface modification of inorganic objects with metal-organic frameworks (MOFs) - organic-inorganic hybrid framework materials with infinite networks - opens wide windows for potential applications. In order to derive a target property, the key is the ability to fine tune the
Serena Berardi et al.
ChemSusChem, 8(21), 3688-3696 (2015-10-02)
Mastering the light-induced four-electron oxidation of water to molecular oxygen is a key step towards the achievement of overall water splitting to produce alternative solar fuels. In this work, we report two rugged molecular pyrazolate-based diruthenium complexes that efficiently catalyze

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