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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-[4-(chloroacetyl)phenyl]-

ClCC(=O)c1ccc(cc1)NC(=O)C Request for Quotation
Chemical Name: Acetamide, N-[4-(chloroacetyl)phenyl]-
CAS Number: 140-49-8
Product Number: AG001BXK(AGN-PC-0JK8QF)
Synonyms:
MDL No:
Molecular Formula: C10H10ClNO2
Molecular Weight: 211.6449

Identification/Properties

Computed Properties
Molecular Weight:
211.645g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
211.04g/mol
Monoisotopic Mass:
211.04g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
222
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Acetamido-2-chloroacetophenone, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly utilized in organic reactions to introduce the acetamido and chloro functional groups into various organic molecules. It serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its unique reactivity and structural properties.One of the main applications of 4-Acetamido-2-chloroacetophenone is in the preparation of complex organic compounds through acylation reactions. By selectively controlling the reaction conditions, chemists can modify the functional groups attached to the phenyl ring, leading to the synthesis of diverse chemical derivatives with specific properties. Additionally, the presence of the acetamido group provides a handle for further derivatization, enabling the synthesis of more complex scaffolds for drug discovery and material science applications.Furthermore, 4-Acetamido-2-chloroacetophenone is commonly employed in the synthesis of heterocyclic compounds, which are essential building blocks in medicinal chemistry and material science. Through strategic transformations involving ring-closing reactions or cross-coupling processes, this compound can be used to construct novel chemical structures with enhanced biological activity or functional properties. Its ability to participate in diverse chemical transformations makes it a valuable tool for chemists seeking to design and synthesize new molecules for various applications.