5,6,7,8-Tetrahidroquinolina - ≥98% , CAS No.10500-57-9

CAS: 10500-57-9 Cat. No.: T108003 Peso molecular: 133.19 Beilstein Registry Number: 20(3/4)2922 Número EC: 234-030-2 PubChem CID: 66335

GRADE & PURITY ≥98%

Synonyms

Z1201617100 | 5,6,7,8-Tetrahydroquinoline | 5,6,7,8-Tetra-hydroquinoline | 5,6,7,8-TETRAHYDRO-QUINOLINE | A801137 | T1150 | EINECS 234-030-2 | UNII-L786AAG56H | AKOS004910439 | InChI=1/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h3,5,7H,1-2,4,6H | SY004991 | Q-20052

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

Z1201617100 | 5, 6, 7, 8-Tetrahydroquinoline | 5, 6, 7, 8-Tetra-hydroquinoline | 5, 6, 7, 8-TETRAHYDRO-QUINOLINE | A801137 | T1150 | EINECS 234-030-2 | UNII-L786AAG56H | AKOS004910439 | InChI=1/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h3, 5, 7H, 1-2, 4, 6H | SY004991 | Q-20052

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488183778
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183778
• Sonrisas canónicas: C1CCC2=C(C1)C=CC=N2
• IUPAC Name: 5,6,7,8-tetrahydroquinoline
• InChIKey: YQDGQEKUTLYWJU-UHFFFAOYSA-N
• INCHI: 1S/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h3,5,7H,1-2,4,6H2
• Isómeros SMILES: C1CCC2=C(C1)C=CC=N2
• PubChem CID: 66335
• Peso molecular: 133.19
• Beilstein: 20(3/4)2922
• Reaxy-Rn: 116148

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Quinolines and derivatives
      • Subclass Hydroquinolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Quinolines and derivatives
• Subclass: Hydroquinolines
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydroquinolines
• Alternative Parents: Pyridines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Tetrahydroquinoline - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.
• 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

Propiedades químicas y físicas

• Solubilidad: Slightly soluble in water
• Sensibilidad: Air sensitive.
• Índice de refracción: 1.54
• Punto de inflamación (°F): 86 °C
• Punto de inflamación (°C): 86°C
• Punto de ebullición (°C): 222°C
• Peso molecular: 133.190 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 133.089 Da
• Monoisotopic Mass: 133.089 Da
• Topological Polar Surface Area: 12.900 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 111.000
• 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

Referencias

1. Chao Huang, Jinhui Li, Deliang Sun, Rui Xuan, Yuying Sui, Tingyu Li, Liang Shang, Guoping Zhang, Rong Sun, Ching Ping Wong.  (2020)  Comprehensive properties study of low-temperature imidized polyimide with curing accelerators.  Journal of Materials Chemistry C,  8  (42): (14886-14894).  [PMID:] [10.1039/D0TC03770B]

2. Wanyi Li, Wenbiao Zhang, He Li, Yi Tang, Yahong Zhang.  (2026)  Zeolite subcrystal-induced formation of short and curved NiMoS2 slabs toward highly efficient hydrodesulfurization.  JOURNAL OF CATALYSIS,      [PMID:] [10.1016/j.jcat.2026.116672]