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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)-

Benzo[h]quinolin-3-ol, 1,2,3,4-tetrahydro-

OC1CNc2c(C1)ccc1c2cccc1 Request for Quotation
Chemical Name: Benzo[h]quinolin-3-ol, 1,2,3,4-tetrahydro-
CAS Number: 5423-67-6
Product Number: AG00DEKU(AGN-PC-0JM1B3)
Synonyms:
MDL No:
Molecular Formula: C13H13NO
Molecular Weight: 199.2484

Identification/Properties

Computed Properties
Molecular Weight:
199.253g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
199.1g/mol
Monoisotopic Mass:
199.1g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
231
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

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


3-Hydroxy-1,2,3,4-tetrahydrobenzo[h]quinoline serves as a valuable building block in chemical synthesis, particularly in the creation of novel pharmaceutical compounds. With its unique structure and functional groups, this compound plays a crucial role in the development of diverse drug molecules with potential therapeutic applications. Chemists utilize 3-Hydroxy-1,2,3,4-tetrahydrobenzo[h]quinoline as a key intermediate in the synthesis of biologically active compounds, enabling the modification and optimization of drug properties for enhanced efficacy and reduced side effects. Its versatile reactivity and compatibility with various synthetic strategies make it a versatile tool in medicinal chemistry research and drug discovery.