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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)-

1-methoxyisoquinoline-3-carboxylic acid

COc1nc(cc2c1cccc2)C(=O)O Request for Quotation
Chemical Name: 1-methoxyisoquinoline-3-carboxylic acid
CAS Number: 1094553-95-3
Product Number: AG0094MY(AGN-PC-0WO5ZE)
Synonyms:
MDL No: MFCD11214764
Molecular Formula: C11H9NO3
Molecular Weight: 203.1941

Identification/Properties

Computed Properties
Molecular Weight:
203.197g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
203.058g/mol
Monoisotopic Mass:
203.058g/mol
Topological Polar Surface Area:
59.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
244
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


1-Methoxyisoquinoline-3-carboxylic acid is a versatile compound widely utilized in chemical synthesis applications. This compound serves as a key building block in the creation of various organic molecules due to its unique structural properties and reactivity. In the field of medicinal chemistry, 1-Methoxyisoquinoline-3-carboxylic acid plays a crucial role in the development of pharmaceuticals and bioactive compounds. Its ability to undergo selective functionalization reactions allows chemists to incorporate specific functionalities into target molecules, enabling the modification of biological activity and pharmacokinetic properties. Additionally, this compound can be used as a precursor in the synthesis of complex natural products and heterocyclic compounds, providing valuable tools for organic chemists in their quest to discover new molecules with potential therapeutic applications.