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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)-

Acetamide, N-[3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl]-N-ethyl-

CCN(c1cccc(c1)C(=O)/C=C/N(C)C)C(=O)C Request for Quotation
Chemical Name: Acetamide, N-[3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl]-N-ethyl-
CAS Number: 96605-66-2
Product Number: AG00IJU7(AGN-PC-07Y4J5)
Synonyms:
MDL No:
Molecular Formula: C15H20N2O2
Molecular Weight: 260.3315

Identification/Properties

Computed Properties
Molecular Weight:
260.337g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
260.152g/mol
Monoisotopic Mass:
260.152g/mol
Topological Polar Surface Area:
40.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
350
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-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide is a key compound used in chemical synthesis for its unique properties. Its application in organic chemistry involves serving as a versatile building block for the creation of complex molecules through various transformations. This compound plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and materials science due to its ability to undergo selective reactions and form important bonds. With its specific structural features, N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide enables precise control over the synthesis process, offering chemists a valuable tool for design and production of advanced organic compounds.