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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-chloro-4-methylphenyl)-

CC(=O)Nc1ccc(c(c1)Cl)C Request for Quotation
Chemical Name: Acetamide, N-(3-chloro-4-methylphenyl)-
CAS Number: 7149-79-3
Product Number: AG003J8I(AGN-PC-0JKH4G)
Synonyms:
MDL No:
Molecular Formula: C9H10ClNO
Molecular Weight: 183.6348

Identification/Properties

Properties
BP:
333.3°C at 760 mmHg
Computed Properties
Molecular Weight:
183.635g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
183.045g/mol
Monoisotopic Mass:
183.045g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
172
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338-P304+P340-P405-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(3-Chloro-4-methylphenyl)acetamide, also known as $name$, is a versatile chemical compound used in various chemical synthesis processes. Its unique molecular structure makes it a valuable reagent in the pharmaceutical, agrochemical, and materials science industries.In chemical synthesis, $name$ is commonly employed as a key intermediate in the production of various pharmaceutical compounds. Its functional groups and reactivity allow for the modification and transformation of complex organic molecules, making it a crucial building block in drug discovery and development.Moreover, $name$ is utilized in the synthesis of specialty chemicals and agrochemicals, where its selective reactivity and compatibility with different reaction conditions enable the efficient creation of novel compounds with specific properties and functions. Its role in these industries contributes to advancements in crop protection, materials design, and green chemistry practices.Overall, the application of N-(3-Chloro-4-methylphenyl)acetamide in chemical synthesis underscores its importance as a key component in creating innovative products and solutions across various industrial sectors.