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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)-

Ethanone, 1-(2-amino-4-methoxy-3-methylphenyl)-

COc1ccc(c(c1C)N)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-(2-amino-4-methoxy-3-methylphenyl)-
CAS Number: 912347-94-5
Product Number: AG00GRGR(AGN-PC-04Z0Y0)
Synonyms:
MDL No:
Molecular Formula: C10H13NO2
Molecular Weight: 179.2157

Identification/Properties

Properties
BP:
336°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
179.219g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
179.095g/mol
Monoisotopic Mass:
179.095g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
193
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2-Amino-4-methoxy-3-methylphenyl)ethanone, also known as $name$, serves as a crucial intermediate in chemical synthesis processes. This compound is widely utilized in organic chemistry for its ability to participate in various reactions, leading to the formation of diverse products with distinct properties.In chemical synthesis, $name$ can act as a versatile building block for the creation of more complex molecules. Its amino and methoxy functional groups enable the introduction of specific functionalities into the final products. Through strategic manipulation of these groups, chemists can tailor the reactivity and properties of the synthesized compounds, catering to specific application requirements.Furthermore, the presence of a methyl substituent on the aromatic ring of $name$ provides opportunities for regioselective reactions, allowing for precise control over the attachment of additional molecular fragments. This feature is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where selectivity and purity are paramount.Overall, the application of 1-(2-Amino-4-methoxy-3-methylphenyl)ethanone in chemical synthesis offers a pathway to the construction of intricate molecular structures with tailored functionalities, making it a valuable tool in the hands of synthetic chemists.