2-methyl-1H-imidazo[4,5-c]pyridin-4-amine - ≥97% , CAS No.1368180-16-8

CAS: 1368180-16-8 Cat. No.: M628640 Peso molecular: 148.17 PubChem CID: 21341987

GRADE & PURITY ≥97%

Synonyms

2-methyl-1H-imidazo[4,5-c]pyridin-4-amine | 1368180-16-8 | SCHEMBL8295987 | F86301

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

2-methyl-1H-imidazo[4, 5-c]pyridin-4-amine | 1368180-16-8 | SCHEMBL8295987 | F86301

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: CC1=NC2=C(N1)C=CN=C2N
• IUPAC Name: 2-methyl-1H-imidazo[4,5-c]pyridin-4-amine
• InChIKey: CMRITTYVUZLJQJ-UHFFFAOYSA-N
• INCHI: 1S/C7H8N4/c1-4-10-5-2-3-9-7(8)6(5)11-4/h2-3H,1H3,(H2,8,9)(H,10,11)
• Isómeros SMILES: CC1=NC2=C(N1)C=CN=C2N
• PubChem CID: 21341987
• Peso molecular: 148.17

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Imidazopyridines
      • Subclass Imidazo-[4,5-c]pyridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Imidazopyridines
• Subclass: Imidazo-[4,5-c]pyridines
• Intermediate Tree Nodes: Not available
• Direct Parent: Imidazo-[4,5-c]pyridines
• Alternative Parents: Aminopyridines and derivatives Imidolactams Imidazoles Heteroaromatic compounds Azacyclic compounds Primary amines Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Imidazo-[4,5-c]pyridine - Aminopyridine - Imidolactam - Pyridine - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as imidazo-[4,5-c]pyridines. These are organic heterocyclic compounds containing an imidazo-[4,5-c]pyridine ring system. Imidazo-[4,5-c]pyridine consists of an imidazole ring fused to a pyridine, so that the three ring nitrogen atoms are at the 1-, 2-, and 5-position, respectively.
• External Descriptors: Not available

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