1. Home
  2. 4-chloro-7-methoxy-1,6-naphthyridine

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-chloro-7-methoxy-1,6-naphthyridine

COc1ncc2c(c1)nccc2Cl Request for Quotation
Chemical Name: 4-chloro-7-methoxy-1,6-naphthyridine
CAS Number: 952138-19-1
Product Number: AG00IIU0(AGN-PC-0CXO2P)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2O
Molecular Weight: 194.6177

Identification/Properties

Computed Properties
Molecular Weight:
194.618g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
194.025g/mol
Monoisotopic Mass:
194.025g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
179
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

Request for Quotation

Customer Feedback

Chemical Structure


4-Chloro-7-methoxy-1,6-naphthyridine is a versatile compound frequently employed in organic chemical synthesis. This chemical serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, 4-Chloro-7-methoxy-1,6-naphthyridine is commonly used as a key intermediate due to its unique structural features and reactive properties. Its ability to undergo various functional group transformations makes it a crucial component in the development of complex organic molecules. This compound can participate in reactions such as nucleophilic substitution, aromatic substitution, and transition metal-catalyzed coupling reactions. Its selective reactivity at the 4-position and the presence of both electron-withdrawing and electron-donating groups allow for precise control over regioselectivity and functional group compatibility in synthetic pathways. Overall, the strategic incorporation of 4-Chloro-7-methoxy-1,6-naphthyridine in chemical synthesis enables chemists to access diverse structural motifs and efficiently construct target molecules with specific biological or physicochemical properties.