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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)-

Octanamide, 3-hydroxy-N-[(3S)-tetrahydro-2-oxo-3-furanyl]-

CCCCCC(CC(=O)N[C@H]1CCOC1=O)O Request for Quotation
Chemical Name: Octanamide, 3-hydroxy-N-[(3S)-tetrahydro-2-oxo-3-furanyl]-
CAS Number: 192883-14-0
Product Number: AG01EOYY(AGN-PC-0O6AY8)
Synonyms:
MDL No:
Molecular Formula: C12H21NO4
Molecular Weight: 243.2994

Identification/Properties

Computed Properties
Molecular Weight:
243.303g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
243.147g/mol
Monoisotopic Mass:
243.147g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
267
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


N-(3-Hydroxyoctanoyl)-L-homoserine lactone is a key molecule used in chemical synthesis for a variety of applications. One important aspect of its use lies in its role as a molecular signal in quorum sensing processes in bacteria. This compound is essential for mediating cell-to-cell communication in bacterial communities, regulating gene expression, and coordinating group behaviors such as biofilm formation and virulence.In chemical synthesis, N-(3-Hydroxyoctanoyl)-L-homoserine lactone serves as a valuable building block for the preparation of novel materials and compounds. Its ability to modulate biological activities makes it a versatile tool for designing specific molecular structures with desired functions. Additionally, its unique chemical properties enable the creation of complex organic molecules that can be further utilized in drug discovery, materials science, and other research fields.Overall, the strategic incorporation of N-(3-Hydroxyoctanoyl)-L-homoserine lactone in chemical synthesis enables the generation of innovative compounds with tailored properties and functionalities, making it an indispensable component in the realm of advanced molecular design and synthesis.