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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, 4-chloro-7-methoxy-2-phenyl-

COc1ccc2c(c1)nc(cc2Cl)c1ccccc1 Request for Quotation
Chemical Name: Quinoline, 4-chloro-7-methoxy-2-phenyl-
CAS Number: 189816-05-5
Product Number: AG002E0G(AGN-PC-0NA08F)
Synonyms:
MDL No:
Molecular Formula: C16H12ClNO
Molecular Weight: 269.7256

Identification/Properties

Computed Properties
Molecular Weight:
269.728g/mol
XLogP3:
4.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
269.061g/mol
Monoisotopic Mass:
269.061g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
293
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-7-methoxy-2-phenylquinoline is a versatile compound widely utilized in chemical synthesis as a key ingredient in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure serves as a valuable building block for the synthesis of complex organic molecules with diverse applications.In chemical synthesis, 4-Chloro-7-methoxy-2-phenylquinoline is often employed as a precursor in the production of biologically active compounds. Its strategic placement within a molecular framework facilitates the introduction of specific functional groups or modifications, allowing for the generation of novel molecules with targeted properties. This compound plays a crucial role in the development of new drugs, agricultural chemicals, and other high-value products with tailored functionalities.Additionally, 4-Chloro-7-methoxy-2-phenylquinoline exhibits favorable reactivity and compatibility with a wide range of synthetic methodologies, enabling chemists to access a diverse array of chemical structures efficiently. Its ability to undergo various transformations and reactions makes it a valuable component in the synthesis of complex organic molecules with precise stereochemistry and functionality.Overall, the application of 4-Chloro-7-methoxy-2-phenylquinoline in chemical synthesis highlights its significance as a versatile and indispensable building block for the creation of advanced materials and biologically active compounds. Its unique properties and reactivity make it a valuable asset in the pursuit of innovative and impactful chemical research and development.