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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)-

(Z)-3-(4-chloroanilino)-N-(4-chlorophenyl)-2-(3-methyl-1,2-oxazol-5-yl)prop-2-enamide

Clc1ccc(cc1)N/C=C(c1onc(c1)C)/C(=O)Nc1ccc(cc1)Cl Request for Quotation
Chemical Name: (Z)-3-(4-chloroanilino)-N-(4-chlorophenyl)-2-(3-methyl-1,2-oxazol-5-yl)prop-2-enamide
CAS Number: 917837-54-8
Product Number: AG00H0B1(AGN-PC-00R8SG)
Synonyms:
MDL No:
Molecular Formula: C19H15Cl2N3O2
Molecular Weight: 388.2473

Identification/Properties

Computed Properties
Molecular Weight:
388.248g/mol
XLogP3:
5.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
387.054g/mol
Monoisotopic Mass:
387.054g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
501
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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-(4-Chlorophenyl)-3-((4-chlorophenyl)amino)-2-(3-methylisoxazol-5-yl)acrylamide serves as a versatile building block in chemical synthesis, particularly in the field of medicinal chemistry and drug development. Due to its unique structure containing both an acrylamide group and a substituted isoxazole ring, this compound demonstrates significant potential for creating novel molecules with diverse biological activities. In synthetic organic chemistry, N-(4-Chlorophenyl)-3-((4-chlorophenyl)amino)-2-(3-methylisoxazol-5-yl)acrylamide can be utilized as a key intermediate for constructing complex organic molecules through various reactions such as cross-coupling, cyclization, and functional group transformations. Its presence can enable the introduction of specific functionalities and structural motifs essential for enhancing the biological properties of target compounds. In drug discovery, this compound plays a crucial role in the synthesis of potential pharmaceutical agents with improved efficacy, selectivity, and pharmacokinetic profiles.