3-methylindolin-7-amine - ≥97% , CAS No.2060027-01-0

CAS: 2060027-01-0 Cat. No.: M631456 Formula: C₉H₁₂N₂ Peso molecolare: 148.2 PubChem CID: 137347341

GRADE & PURITY ≥97%

Synonyms

3-Methylindolin-7-amine | 2060027-01-0 | 3-methyl-2,3-dihydro-1H-indol-7-amine | MFCD30499974 | PB41769 | AS-78875 | EN300-338933 | P20144

Storage

Room temperature

Shipped In

Normal

Specifications

Sinonimi

3-Methylindolin-7-amine | 2060027-01-0 | 3-methyl-2,3-dihydro-1H-indol-7-amine | MFCD30499974 | PB41769 | AS-78875 | EN300-338933 | P20144

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥97%

Nomi e identificatori

• Sorrisi canonici: CC1CNC2=C1C=CC=C2N
• IUPAC Name: 3-methyl-2,3-dihydro-1H-indol-7-amine
• InChIKey: BXLIZFJXBSLUIY-UHFFFAOYSA-N
• INCHI: 1S/C9H12N2/c1-6-5-11-9-7(6)3-2-4-8(9)10/h2-4,6,11H,5,10H2,1H3
• PubChem CID: 137347341
• Peso molecolare: 148.2

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Indoles and derivatives
      • Subclass Indolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Indoles and derivatives
• Subclass: Indolines
• Intermediate Tree Nodes: Not available
• Direct Parent: Indolines
• Alternative Parents: Secondary alkylarylamines Benzenoids Pyrrolines Dialkylamines Azacyclic compounds Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Dihydroindole - Secondary aliphatic/aromatic amine - Benzenoid - Pyrroline - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as indolines. These are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.
• 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