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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)-

4,8-Isoquinolinediol, 1,2,3,4-tetrahydro-2-methyl-

CN1CC(O)c2c(C1)c(O)ccc2 Request for Quotation
Chemical Name: 4,8-Isoquinolinediol, 1,2,3,4-tetrahydro-2-methyl-
CAS Number: 23824-25-1
Product Number: AG00C2WE(AGN-PC-0O84SS)
Synonyms:
MDL No:
Molecular Formula: C10H13NO2
Molecular Weight: 179.21572

Identification/Properties

Computed Properties
Molecular Weight:
179.219g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
179.095g/mol
Monoisotopic Mass:
179.095g/mol
Topological Polar Surface Area:
43.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
186
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,2,3,4-Tetrahydro-2-methyl-4,8-isoquinolinediol is a versatile compound widely utilized in chemical synthesis. Specifically, this compound is employed as a key intermediate in the production of various pharmaceuticals and fine chemicals. Its unique chemical structure and reactivity make it a valuable building block for the synthesis of complex molecules with significant biological activities.In chemical synthesis, 1,2,3,4-Tetrahydro-2-methyl-4,8-isoquinolinediol serves as a vital starting material for the preparation of pharmaceutical agents such as antiarrhythmic drugs and anti-cancer compounds. Furthermore, its cyclic structure allows for diverse functionalization, enabling the introduction of different chemical groups to modulate the properties of the final product. This compound's role in the creation of structurally complex molecules highlights its importance in the field of medicinal chemistry and drug discovery.Additionally, 1,2,3,4-Tetrahydro-2-methyl-4,8-isoquinolinediol is utilized in the synthesis of agrochemicals, dyes, and other specialty chemicals. Its versatile reactivity and ability to participate in various chemical transformations make it an indispensable component in the toolkit of synthetic chemists. By leveraging the unique properties of this compound, researchers can access novel chemical entities with potential applications across different industries.