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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-(1-phenylethyl)-

ClCC(=O)NC(c1ccccc1)C Request for Quotation
Chemical Name: Acetamide, 2-chloro-N-(1-phenylethyl)-
CAS Number: 13230-80-3
Product Number: AG0010IS(AGN-PC-0JNBKQ)
Synonyms:
MDL No:
Molecular Formula: C10H12ClNO
Molecular Weight: 197.6614

Identification/Properties

Computed Properties
Molecular Weight:
197.662g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
197.061g/mol
Monoisotopic Mass:
197.061g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
166
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


2-Chloro-N-(1-phenylethyl)acetamide, also known as $name$, is a versatile compound widely utilized in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a valuable building block in the construction of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties and reactivity.In chemical synthesis, 2-Chloro-N-(1-phenylethyl)acetamide acts as a key intermediate in the production of numerous organic compounds. Its functional groups enable it to participate in a wide range of reactions, including nucleophilic substitution, acylation, and cross-coupling reactions. By selectively modifying the chloro group or the phenylethyl group, chemists can access a diverse array of derivatives with tailored properties and functionalities.One of the primary applications of 2-Chloro-N-(1-phenylethyl)acetamide is in the synthesis of bioactive molecules such as pharmaceutical drugs. Its incorporation into complex molecular structures allows for the efficient assembly of drug candidates with potential therapeutic benefits. Furthermore, this compound plays a crucial role in the development of new materials, dyes, and other specialty chemicals through strategic functionalization and elaboration strategies.Overall, the strategic use of 2-Chloro-N-(1-phenylethyl)acetamide in chemical synthesis enables chemists to access a vast chemical space and create novel compounds with diverse applications, showcasing its significance in modern organic chemistry and research endeavors.