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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-Quinolinol, 1,2,3,4-tetrahydro-

OC1CCNc2c1cccc2 Request for Quotation
Chemical Name: 4-Quinolinol, 1,2,3,4-tetrahydro-
CAS Number: 24206-39-1
Product Number: AG00BH2X(AGN-PC-05RDRL)
Synonyms:
MDL No:
Molecular Formula: C9H11NO
Molecular Weight: 149.1897

Identification/Properties

Computed Properties
Molecular Weight:
149.193g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
149.084g/mol
Monoisotopic Mass:
149.084g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
138
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


1,2,3,4-Tetrahydroquinolin-4-ol is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a key building block in the design and synthesis of various bioactive molecules and pharmaceutical drugs. Its cyclic structure and functional groups make it a valuable intermediate in the production of diverse organic compounds.One important application of 1,2,3,4-Tetrahydroquinolin-4-ol is in the preparation of heterocyclic derivatives. By utilizing its cyclohexane ring and hydroxyl group, chemists can modify its structure through various chemical reactions to introduce different substituents or functional groups. This enables the synthesis of complex heterocyclic compounds with diverse biological activities, such as antiviral, antibacterial, and anticancer agents.Furthermore, 1,2,3,4-Tetrahydroquinolin-4-ol can participate in a range of organic transformations, including oxidation, reduction, alkylation, and acylation reactions. These reactions allow for the creation of new carbon-carbon and carbon-heteroatom bonds, leading to the synthesis of structurally diverse molecules with potential therapeutic applications.Overall, the versatility and reactivity of 1,2,3,4-Tetrahydroquinolin-4-ol make it a valuable tool in chemical synthesis, enabling the creation of novel compounds with biological significance and pharmaceutical potential.