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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, 2-chloro-4,8-dimethyl-

Clc1cc(C)c2c(n1)c(C)ccc2 Request for Quotation
Chemical Name: Quinoline, 2-chloro-4,8-dimethyl-
CAS Number: 3913-17-5
Product Number: AG0076HY(AGN-PC-0JO1KO)
Synonyms:
MDL No:
Molecular Formula: C11H10ClN
Molecular Weight: 191.6568

Identification/Properties

Computed Properties
Molecular Weight:
191.658g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
191.05g/mol
Monoisotopic Mass:
191.05g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
183
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4,8-dimethylquinoline is a valuable compound in chemical synthesis due to its versatile applications. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials. With its unique structure and reactivity, this compound can be utilized as a precursor in the synthesis of heterocyclic compounds, which are essential in pharmaceutical research and development. Additionally, 2-Chloro-4,8-dimethylquinoline is a potent intermediate in the production of dyes and pigments, adding vibrant color to numerous products. Its role in chemical synthesis extends to the field of materials science, where it can be incorporated into polymers and coatings, imparting specific properties and functionalities. By leveraging the synthetic potential of 2-Chloro-4,8-dimethylquinoline, researchers and chemists can access a wide range of applications across various industries, making it a valuable tool in modern chemistry.