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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Quinoline, 6,8-dimethyl-

Cc1cc2cccnc2c(c1)C Request for Quotation
Chemical Name: Quinoline, 6,8-dimethyl-
CAS Number: 2436-93-3
Product Number: AG00BECT(AGN-PC-0JLPF3)
Synonyms:
MDL No:
Molecular Formula: C11H11N
Molecular Weight: 157.21174

Identification/Properties

Properties
MP:
51.53°C (estimate)
BP:
268.55°C
Storage:
Room Temperature;
Form:
Solid
Refractive Index:
1.6094 (estimate)
Computed Properties
Molecular Weight:
157.216g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
157.089g/mol
Monoisotopic Mass:
157.089g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
155
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,8-Dimethylquinoline is a versatile compound commonly used in chemical synthesis as a building block for various organic molecules. With its unique structure and reactivity, this compound is particularly valuable in the pharmaceutical and agrochemical industries.One of the key applications of 6,8-Dimethylquinoline is in the synthesis of heterocyclic compounds, which are essential in drug development. By incorporating this compound into the molecular structure of pharmaceutical agents, researchers can modulate their biological activity and enhance their efficacy. Additionally, 6,8-Dimethylquinoline can serve as a precursor in the preparation of complex molecules such as alkaloids and dyes.Furthermore, this compound can be utilized as a ligand in coordination chemistry, where it can form stable complexes with metal ions. These metal complexes have been employed in catalytic reactions, photochemistry, and material science applications. Additionally, 6,8-Dimethylquinoline derivatives can exhibit luminescent properties, making them useful in the development of sensors and optoelectronic devices.Overall, 6,8-Dimethylquinoline plays a crucial role in advancing chemical synthesis by enabling the construction of diverse organic structures with unique properties and applications.