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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-Quinolinecarboxamide, 3-hydroxy-2-phenyl-N-[(1S)-1-phenylpropyl]-

CC[C@@H](c1ccccc1)NC(=O)c1c(O)c(nc2c1cccc2)c1ccccc1 Request for Quotation
Chemical Name: 4-Quinolinecarboxamide, 3-hydroxy-2-phenyl-N-[(1S)-1-phenylpropyl]-
CAS Number: 174636-32-9
Product Number: AG001ZU9(AGN-PC-0O4XVX)
Synonyms:
MDL No:
Molecular Formula: C25H22N2O2
Molecular Weight: 382.4544

Identification/Properties

Properties
MP:
115 - 120°C
BP:
580.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
382.463g/mol
XLogP3:
5.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
382.168g/mol
Monoisotopic Mass:
382.168g/mol
Topological Polar Surface Area:
62.2A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
527
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P264-P270-P301+P310+P330-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-Hydroxy-2-phenyl-N-[(1S)-1-phenylpropyl]-4-quinolinecarboxamide is a versatile reagent commonly used in chemical synthesis. Its unique structure and reactivity make it a valuable tool in the creation of various organic compounds.One key application of this compound in chemical synthesis is as a building block for the synthesis of novel pharmaceuticals. By incorporating 3-Hydroxy-2-phenyl-N-[(1S)-1-phenylpropyl]-4-quinolinecarboxamide into the molecular structure of a target compound, chemists can introduce specific functional groups or stereochemistry that are crucial for enhancing the desired biological activity of the final product.Additionally, this compound can serve as a valuable intermediate in the synthesis of bioactive molecules such as natural products or agrochemicals. Its ability to undergo various chemical transformations allows for the efficient construction of complex molecular architectures, enabling researchers to explore new chemical space and discover compounds with potentially valuable properties.Overall, 3-Hydroxy-2-phenyl-N-[(1S)-1-phenylpropyl]-4-quinolinecarboxamide plays a vital role in chemical synthesis, offering chemists a powerful tool for the design and creation of diverse organic compounds with potential applications in pharmaceuticals, materials science, and other fields.