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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-bromo-2-chloro-4-methyl-

Brc1ccc2c(c1)c(C)cc(n2)Cl Request for Quotation
Chemical Name: Quinoline, 6-bromo-2-chloro-4-methyl-
CAS Number: 3913-19-7
Product Number: AG00C0O2(AGN-PC-0LGFUT)
Synonyms:
MDL No:
Molecular Formula: C10H7BrClN
Molecular Weight: 256.5263

Identification/Properties

Properties
MP:
140℃
BP:
347.6°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
256.527g/mol
XLogP3:
4.2
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


6-Bromo-2-chloro-4-methylquinoline, a versatile compound widely used in chemical synthesis, plays a crucial role in the development of novel molecules with diverse applications. Its unique structure and reactivity make it a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and materials. By serving as a key intermediate in organic reactions, this compound enables the creation of complex molecular structures and facilitates the modification of functional groups. Additionally, its presence in the chemical synthesis process allows for the exploration of new pathways and strategies in the development of biologically active compounds and advanced materials. Overall, the application of 6-Bromo-2-chloro-4-methylquinoline in chemical synthesis offers a promising avenue for the discovery and production of innovative compounds with enhanced properties and applications.