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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-7-methoxy-

COc1ccc2c(c1)nc(cc2)Cl Request for Quotation
Chemical Name: Quinoline, 2-chloro-7-methoxy-
CAS Number: 49609-15-6
Product Number: AG0037FG(AGN-PC-0OB0C7)
Synonyms:
MDL No:
Molecular Formula: C10H8ClNO
Molecular Weight: 193.6296

Identification/Properties

Properties
MP:
97-98℃
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
193.63g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
193.029g/mol
Monoisotopic Mass:
193.029g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
176
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


2-Chloro-7-methoxyquinoline is a versatile chemical compound that finds significant application in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure, 2-Chloro-7-methoxyquinoline demonstrates excellent reactivity and selectivity in a range of synthetic transformations.In organic synthesis, 2-Chloro-7-methoxyquinoline is commonly utilized as a key intermediate in the production of novel drug candidates, particularly in the development of antimalarial and antimicrobial agents. Its functional group reactivity allows for efficient modifications and derivatizations, enabling chemists to tailor the compound's properties to meet specific requirements in drug design.Furthermore, 2-Chloro-7-methoxyquinoline plays a crucial role in the synthesis of complex heterocyclic compounds, which are essential in medicinal chemistry and material science. Its structural characteristics contribute to the formation of diverse molecular scaffolds, facilitating the creation of biologically active compounds with potential therapeutic benefits.Overall, the versatile nature of 2-Chloro-7-methoxyquinoline makes it an indispensable tool for chemists engaged in the synthesis of valuable chemicals and pharmaceuticals.