1. Home
  2. 4-bromo-6-chloro-8-methylquinoline

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

4-bromo-6-chloro-8-methylquinoline

Clc1cc(C)c2c(c1)c(Br)ccn2 Request for Quotation
Chemical Name: 4-bromo-6-chloro-8-methylquinoline
CAS Number: 927800-42-8
Product Number: AG006E0Y(AGN-PC-01A9R8)
Synonyms:
MDL No:
Molecular Formula: C10H7BrClN
Molecular Weight: 256.5263

Identification/Properties

Computed Properties
Molecular Weight:
256.527g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
254.945g/mol
Monoisotopic Mass:
254.945g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
188
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Bromo-6-chloro-8-methylquinoline is a versatile compound widely used in chemical synthesis. Its unique structure makes it a valuable building block for the creation of various chemical compounds with specialized properties and functions. In organic synthesis, 4-Bromo-6-chloro-8-methylquinoline serves as an important intermediate in the production of pharmaceuticals, agrochemicals, and materials with advanced applications. Its distinct bromo and chloro substituents allow for selective functionalization and modification of the quinoline ring system, enabling the synthesis of diverse molecular structures. Furthermore, the presence of the methyl group enhances the compound's reactivity and compatibility with other reagents, facilitating efficient transformations in complex chemical reactions. Overall, 4-Bromo-6-chloro-8-methylquinoline plays a crucial role in expanding the repertoire of available chemical building blocks and driving innovation in the field of chemical synthesis.