Picolinamide - 10mM in DMSO , CAS No.1452-77-3

CAS: 1452-77-3 Cat. No.: P421668 Fórmula: C₆H₆N₂O Peso molecular: 122.12 Beilstein Registry Number: 22(3/4)311 Número EC: 215-921-5 PubChem CID: 15070

GRADE & PURITY 10mM in DMSO

Synonyms

C01950 | NSC 524473 | alpha-Picolinamide | PICOLINAMIDE [INCI] | 2-Carbamoylpyridine | Picolinamide; 2-Pyridinecarboxamide | pyridine amide | s4710 | .alpha.-Pyridinecarboxamide | J-008082 | 2-Pyridinecarboxamide | 2-pyridine-carboxamide | alpha - picolin

Storage

Protected from light,Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

Picolinamide is potential inhibitor of poly (ADP-ribose) synthetase of nuclei from rat pancreatic islet cells. It acts as bidentate ligand and forms complexes with lanthanide nitrates, thiocyanates and perchlorates. Picolinamide can be used as template in preparation of molecular imprinting polymer. Picolinamide can be used in a study to evaluate kinetics and mechanism of liberation of picolinamide from chromium(III)-picolinamide complexes in perchloric acid.
Picolinamide was used as template in preparation of molecular imprinting polymer1. Picolinamide was used in a study to evaluate kinetics and mechanism of liberation of picolinamide from chromium(III)-picolinamide complexes in HClO42.

Specifications

Sinónimos

C01950 | NSC 524473 | alpha-Picolinamide | PICOLINAMIDE [INCI] | 2-Carbamoylpyridine | Picolinamide; 2-Pyridinecarboxamide | pyridine amide | s4710 | .alpha.-Pyridinecarboxamide | J-008082 | 2-Pyridinecarboxamide | 2-pyridine-carboxamide | alpha - picolin

Especificaciones y pureza

10mM in DMSO

Mecanismos bioquímicos y fisiológicos

Pyridylamide is a potential inhibitor of ADP ribose synthetase. Pyridinamides act as bidentate ligands and form complexes with lanthanide nitrates, thiocyanates and perchlorates.

Condiciones de almacenamiento de almacenamiento

Protected from light,Store at -80°C

Enviado en

Dry ice packs + Cold packs

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

Pubchem Sid

528770781

Sonrisas canónicas

C1=CC=NC(=C1)C(=O)N

IUPAC Name

pyridine-2-carboxamide

InChIKey

IBBMAWULFFBRKK-UHFFFAOYSA-N

INCHI

1S/C6H6N2O/c7-6(9)5-3-1-2-4-8-5/h1-4H,(H2,7,9)

Isómeros SMILES

C1=CC=NC(=C1)C(=O)N

WGK Alemania

3

PubChem CID

15070

Peso molecular

122.12

Beilstein

22(3/4)311

Reaxy-Rn

109617

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Pyridines and derivatives
      • Subclass Pyridinecarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Pyridines and derivatives
• Subclass: Pyridinecarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridinecarboxamides
• Alternative Parents: 2-heteroaryl carboxamides Heteroaromatic compounds Primary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyridinecarboxamide - 2-heteroaryl carboxamide - Heteroaromatic compound - Primary carboxylic acid amide - Carboxamide group - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyridinecarboxamides. These are compounds containing a pyridine ring bearing a carboxamide.
• External Descriptors: pyridinecarboxamide

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Punto de ebullición (°C): 143 °C/20 mmHg
• Punto de fusión (°C): 105 °C
• Peso molecular: 122.120 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 122.048 Da
• Monoisotopic Mass: 122.048 Da
• Topological Polar Surface Area: 56.000 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 114.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1