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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, 2-chloro-N-phenyl-

ClCC(=O)Nc1ccccc1 Request for Quotation
Chemical Name: Acetamide, 2-chloro-N-phenyl-
CAS Number: 587-65-5
Product Number: AG003H2Y(AGN-PC-0JKA21)
Synonyms:
MDL No:
Molecular Formula: C8H8ClNO
Molecular Weight: 169.6082

Identification/Properties

Properties
MP:
136-139 °C(lit.)
BP:
340 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
169.608g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
169.029g/mol
Monoisotopic Mass:
169.029g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
132
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-N-phenylacetamide, a chemical compound utilized in chemical synthesis processes, serves as a versatile building block in the pharmaceutical and agrochemical industries. Its strategic incorporation in the synthesis of various organic compounds allows for the production of novel drugs, pesticides, and other valuable chemicals. With its unique structural properties and reactivity, 2-Chloro-N-phenylacetamide enables the formation of diverse molecular structures, paving the way for the development of innovative compounds with potential applications in the fields of medicine and agriculture. This compound plays a crucial role in the creation of new synthetic pathways and the enhancement of existing methodologies, making it a valuable tool for researchers and chemists alike.