GRADE & PURITY ≥98%

Synonyms

M0419 | Quinoline, 8-methyl- | DTXSID8020888 | 1199266-77-7 | DTXCID80888 | MFCD00006810 | MLS002303012 | NISTC611325 | NSC 9409 | I11487 | Quinoline, 8-methyl-, labeled with deuterium | SCHEMBL256942 | HMS3039E09 | 8-methyl quinoline | K97B12J636 | FT-06

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Descripción general

Product Description

Tumorigenic potential of 8-methylquinoline has been evaluated in newborn CD-1 mice and Sprague-Dawley rats

Product Application

8-Methylquinoline has been used in preparation of osmium chloridophosphine complexes, as quinoline carbene tautomers.

Specifications

Sinónimos

M0419 | Quinoline, 8-methyl- | DTXSID8020888 | 1199266-77-7 | DTXCID80888 | MFCD00006810 | MLS002303012 | NISTC611325 | NSC 9409 | I11487 | Quinoline, 8-methyl-, labeled with deuterium | SCHEMBL256942 | HMS3039E09 | 8-methyl quinoline | K97B12J636 | FT-06

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

FedEx DG Service

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

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488181473
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181473
• Sonrisas canónicas: CC1=C2C(=CC=C1)C=CC=N2
• IUPAC Name: 8-methylquinoline
• InChIKey: JRLTTZUODKEYDH-UHFFFAOYSA-N
• INCHI: 1S/C10H9N/c1-8-4-2-5-9-6-3-7-11-10(8)9/h2-7H,1H3
• Isómeros SMILES: CC1=C2C(=CC=C1)C=CC=N2
• WGK Alemania: 3
• RTECS: VC0562000
• Peso molecular: 143.19
• Beilstein: 111340
• Reaxy-Rn: 111340
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=111340&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Quinolines and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Quinolines and derivatives
• Alternative Parents: Pyridines and derivatives Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Quinoline - Benzenoid - 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 quinolines and derivatives. These are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.
• External Descriptors: methylquinoline

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

Objetivos asociados (humanos)

HCT-116 (91556 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)

Discover Target: ATAD5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Plasmodium falciparum (966862 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water 0.1-0.5 g/100 mL at 17°C
• Sensibilidad: air sensitive
• Índice de refracción: 1.62
• Punto de inflamación (°F): 221 °F
• Punto de inflamación (°C): 105 °C
• Punto de ebullición (°C): 248°C
• Punto de fusión (°C): -80°C
• Peso molecular: 143.180 g/mol
• XLogP3: 2.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 143.073 Da
• Monoisotopic Mass: 143.073 Da
• Topological Polar Surface Area: 12.900 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 133.000
• 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]