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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-methoxyphenyl)-

ClCC(=O)Nc1cccc(c1)OC Request for Quotation
Chemical Name: Acetamide, 2-chloro-N-(3-methoxyphenyl)-
CAS Number: 17641-08-6
Product Number: AG0024ND(AGN-PC-0JKK7T)
Synonyms:
MDL No:
Molecular Formula: C9H10ClNO2
Molecular Weight: 199.6342

Identification/Properties

Computed Properties
Molecular Weight:
199.634g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
199.04g/mol
Monoisotopic Mass:
199.04g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
175
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P264-P270-P301+P312-P330-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-N-(3-methoxyphenyl)acetamide, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is commonly employed in the development of pharmaceuticals and agrochemicals due to its valuable properties and functional groups. Within chemical synthesis, $name$ acts as a key intermediate in the production of various organic compounds through efficient and selective reactions. Its strategic incorporation allows for the introduction of specific functionalities and structural motifs, facilitating the design and optimization of target molecules with desired activities. Moreover, the presence of the chloro and methoxy substituents on the aromatic ring provides unique opportunities for further derivatization and diversification to access structurally diverse compounds with potential biological or industrial significance. By harnessing the reactivity and versatility of 2-Chloro-N-(3-methoxyphenyl)acetamide, chemists can intricately manipulate molecular structures and advance the frontier of chemical synthesis.