I17508
Isonicotinic acid
99%
Synonym(s):
4-Picolinic acid, Pyridine-4-carboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C6H5NO2
CAS Number:
Molecular Weight:
123.11
Beilstein:
109599
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
99%
form
powder
technique(s)
cell culture | plant: suitable
mp
≥300 °C (lit.)
≥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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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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
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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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)
Antimalarial Cation-dimers Synthesized in Two Steps from an Inexpensive Starting Material, Isonicotinic Acid
Motoshima K, et al.
ChemMedChem, 2(10), 1527-1532 (2007)
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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