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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-(3,5-dimethoxyphenyl)-

ClCC(=O)Nc1cc(OC)cc(c1)OC Request for Quotation
Chemical Name: Acetamide, 2-chloro-N-(3,5-dimethoxyphenyl)-
CAS Number: 66932-96-5
Product Number: AG00FB1L(AGN-PC-0KEJZP)
Synonyms:
MDL No:
Molecular Formula: C10H12ClNO3
Molecular Weight: 229.6602

Identification/Properties

Computed Properties
Molecular Weight:
229.66g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
229.051g/mol
Monoisotopic Mass:
229.051g/mol
Topological Polar Surface Area:
47.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
201
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-(3,5-dimethoxyphenyl)acetamide, often referred to as $name$, is a versatile compound widely utilized in chemical synthesis processes. Due to its unique molecular structure, this compound exhibits excellent reactivity and selectivity in various reactions, making it a valuable tool in organic chemistry.One prominent application of 2-Chloro-N-(3,5-dimethoxyphenyl)acetamide is in the field of pharmaceutical chemistry. This compound serves as a key intermediate in the synthesis of biologically active molecules and pharmaceutical agents. By incorporating $name$ into a synthetic route, chemists can access a diverse range of structurally complex compounds with potential therapeutic properties.Additionally, 2-Chloro-N-(3,5-dimethoxyphenyl)acetamide plays a crucial role in the preparation of agrochemicals and specialty chemicals. Its ability to undergo selective functionalization reactions enables the efficient assembly of intricate chemical structures essential for the development of novel agrochemicals and specialty chemicals.Furthermore, this compound is utilized in the synthesis of advanced materials, including polymers, dyes, and catalysts. The presence of the chloro and dimethoxy functional groups in 2-Chloro-N-(3,5-dimethoxyphenyl)acetamide imparts specific properties to the resulting materials, such as enhanced stability, reactivity, or color characteristics.Overall, the versatile nature of 2-Chloro-N-(3,5-dimethoxyphenyl)acetamide makes it a valuable building block in chemical synthesis, offering chemists a wide range of possibilities for the creation of diverse molecular structures with potential applications in various industries.