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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)-

7-Isoquinolinol, 3-methyl-

Oc1ccc2c(c1)cnc(c2)C Request for Quotation
Chemical Name: 7-Isoquinolinol, 3-methyl-
CAS Number: 63485-73-4
Product Number: AG00EK6L(AGN-PC-0NILVD)
Synonyms:
MDL No:
Molecular Formula: C10H9NO
Molecular Weight: 159.1846

Identification/Properties

Properties
MP:
252-255℃
BP:
329.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
159.188g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
159.068g/mol
Monoisotopic Mass:
159.068g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
160
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:
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


The versatile chemical compound 3-Methylisoquinolin-7-ol plays a crucial role in chemical synthesis, particularly in the realms of pharmaceuticals and materials science. Its unique structure allows for a wide range of applications in the creation of novel molecules and materials. In organic synthesis, 3-Methylisoquinolin-7-ol serves as a valuable building block in the construction of complex organic structures, facilitating the formation of intricate molecular frameworks with specific functional properties. Additionally, this compound can be utilized in the development of various medicinal compounds, serving as a key intermediate in the synthesis of pharmaceutical agents with potential therapeutic benefits. Its incorporation into chemical reactions enables the selective modification of molecules, leading to the creation of tailored compounds with enhanced properties for specific applications. Furthermore, the diverse reactivity of 3-Methylisoquinolin-7-ol makes it a valuable tool for the exploration of new chemical transformations and the discovery of innovative synthetic pathways. By harnessing the unique capabilities of this compound, researchers and chemists can unlock new possibilities in the realm of chemical synthesis, paving the way for advancements in drug discovery, materials science, and beyond.