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6-Methylquinoline - 98%, high purity , CAS No.91-62-3

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6-Methylquinoline - 98%, high purity , CAS No.91-62-3

1 Citations

COA

Grade & Purity:

≥98%

Cas Number: 91-62-3
Molecular Weight: 143.19
Beilstein Registry Number: 110336
EC Number: 200-677-4
MDL number: MFCD00006804
PubChem CID: 7059
PubChem SID: 488180267

In stock

Item Number

M109545

Grouped product items
SKU	Size	Availability	Price
M109545-5g	5g	3	$12.90
M109545-25g	25g	3	$49.90
M109545-100g	100g	1	$152.90
M109545-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$688.90

View related series

Pyridines (1259) Six-Membered Heterocyclic Compounds (1696)

Basic Description

Synonyms	6-Methylquinoline, >=98%, FG \| p-Toluquinoline \| NCGC00091226-02 \| p-Tolliquinoline \| AI3-08869 \| HMS3039C14 \| Quinoline, 6-methyl- \| MLS002303009 \| Quinoline, 6-methyl- (8CI,9CI) \| Tox21_300320 \| CCRIS 407 \| EINECS 202-084-6 \| NCGC00091226-03 \| FEMA 2744
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	6-Methylquinoline undergoes biodegradation by quinoline-degrading culture of Pseudomonas putida.
Storage Temp	Protected from light,Argon charged
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Quinolines and derivatives

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	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
Description	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	Not available
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

Associated Targets(Human)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

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

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488180267
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180267
IUPAC Name	6-methylquinoline
INCHI	InChI=1S/C10H9N/c1-8-4-5-10-9(7-8)3-2-6-11-10/h2-7H,1H3
InChIKey	LUYISICIYVKBTA-UHFFFAOYSA-N
Smiles	CC1=CC2=C(C=C1)N=CC=C2
Isomeric SMILES	CC1=CC2=C(C=C1)N=CC=C2
WGK Germany	3
RTECS	AI5950000
Molecular Weight	143.19
Beilstein	110336
Reaxy-Rn	110336
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=110336&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot Number	Certificate Type	Date	Item
D2126282	Certificate of Analysis	Feb 07, 2025	M109545
E2406149	Certificate of Analysis	Mar 25, 2024	M109545
E2406155	Certificate of Analysis	Mar 25, 2024	M109545
C2027066	Certificate of Analysis	Jan 18, 2024	M109545
E2323965	Certificate of Analysis	Dec 29, 2022	M109545
E23231153	Certificate of Analysis	Dec 29, 2022	M109545
E2323969	Certificate of Analysis	Dec 29, 2022	M109545
E23231158	Certificate of Analysis	Dec 29, 2022	M109545
E2323921	Certificate of Analysis	Dec 29, 2022	M109545
E2323925	Certificate of Analysis	Dec 29, 2022	M109545
E2323860	Certificate of Analysis	Dec 29, 2022	M109545

Show more⌵

Chemical and Physical Properties

Solubility	Not miscible or difficult to mix with water.
Sensitivity	Air & Light Sensitive
Refractive Index	1.615～1.616
Flash Point(°F)	235.4 °F
Flash Point(°C)	113 °C
Boil Point(°C)	259°C
Melt Point(°C)	22°C
Molecular Weight	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 Å²
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yufen Wang, Yantao Wang, Yongqing Ma, Asma Mohmmad Elsharif, Chen Zhang, Weiran Yang, Christophe Len. (2024) A transition-metal-free catalytic reduction of benzylic alcohols and alkenes and N-formylation of nitroarenes mediated by iodide ions and formic acid. NEW JOURNAL OF CHEMISTRY,

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