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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)-

3-chloro-7-methoxyquinoline

COc1ccc2c(c1)ncc(c2)Cl Request for Quotation
Chemical Name: 3-chloro-7-methoxyquinoline
CAS Number: 858279-19-3
Product Number: AG004O8I(AGN-PC-0DACV7)
Synonyms:
MDL No:
Molecular Formula: C10H8ClNO
Molecular Weight: 193.6296

Identification/Properties

Properties
BP:
299.804°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
193.63g/mol
XLogP3:
3
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chloro-7-methoxyquinoline is a valuable chemical intermediate widely utilized in organic synthesis. With its unique structure and reactivity, this compound plays a crucial role in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, 3-Chloro-7-methoxyquinoline serves as a versatile building block for the creation of complex molecules. Its chloro and methoxy substituents offer strategic functional groups that can be selectively modified or utilized in different reactions. By incorporating this compound into a synthesis route, chemists can introduce specific functionalities at precise positions in the target molecule, enhancing their control over the synthetic process.The presence of the quinoline scaffold in 3-Chloro-7-methoxyquinoline further adds to its synthetic utility. Quinoline derivatives are known for their diverse biological activities, making them valuable components in designing new drugs and bioactive compounds. By incorporating 3-Chloro-7-methoxyquinoline into a molecule, researchers can potentially impart desired pharmacological properties, making it an essential reagent in medicinal chemistry research.Overall, the application of 3-Chloro-7-methoxyquinoline in chemical synthesis opens up possibilities for the efficient and targeted construction of complex organic molecules with specific functionalities, facilitating advancements in drug discovery, materials science, and other fields of chemical research.