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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)-

2-Propenamide, N-(2-chlorophenyl)-3-phenyl-

O=C(Nc1ccccc1Cl)C=Cc1ccccc1 Request for Quotation
Chemical Name: 2-Propenamide, N-(2-chlorophenyl)-3-phenyl-
CAS Number: 73108-79-9
Product Number: AG00FW0N(AGN-PC-0JONOO)
Synonyms:
MDL No: MFCD00157758
Molecular Formula: C15H12ClNO
Molecular Weight: 257.7149

Identification/Properties

Computed Properties
Molecular Weight:
257.717g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
257.061g/mol
Monoisotopic Mass:
257.061g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
297
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(2-Chlorophenyl)cinnamamide, also known as $name$, is a versatile compound widely utilized in chemical synthesis for various applications. This compound serves as a key building block in the preparation of organic compounds due to its reactive nature and structural flexibility. It is commonly employed as a substrate in organic reactions to introduce the 2-chlorophenyl and cinnamamide moieties into target molecules. Additionally, $name$ can undergo various functionalization reactions, such as acylation, alkylation, and condensation, to form diverse chemical products with tailored properties. Its presence in chemical synthesis processes often contributes to the development of new materials, pharmaceuticals, and agrochemicals, highlighting its significance in modern synthetic chemistry.