
CAS 88135-26-6
:Methyl 4-amino-2,6-dichlorobenzeneacetate
Description:
Methyl 4-amino-2,6-dichlorobenzeneacetate, identified by its CAS number 88135-26-6, is an organic compound characterized by its aromatic structure and the presence of both amino and ester functional groups. This compound features a dichlorobenzene ring, which contributes to its chemical stability and potential reactivity. The amino group (-NH2) is typically associated with basic properties and can participate in various chemical reactions, including nucleophilic substitutions. The ester group (-COOCH3) indicates that it can undergo hydrolysis, leading to the formation of the corresponding acid and alcohol. Methyl 4-amino-2,6-dichlorobenzeneacetate may exhibit biological activity, making it of interest in pharmaceutical research. Its physical properties, such as solubility and melting point, can vary based on environmental conditions and the presence of other substances. Overall, this compound's unique structure and functional groups make it a subject of interest in both synthetic chemistry and potential applications in medicinal chemistry.
Formula:C9H9Cl2NO2
InChI:InChI=1S/C9H9Cl2NO2/c1-14-9(13)4-6-7(10)2-5(12)3-8(6)11/h2-3H,4,12H2,1H3
InChI key:InChIKey=CGTBRJDCBUVUBG-UHFFFAOYSA-N
SMILES:C(C(OC)=O)C1=C(Cl)C=C(N)C=C1Cl
Synonyms:- Methyl 4-amino-2,6-dichlorobenzeneacetate
- Benzeneacetic acid, 4-amino-2,6-dichloro-, methyl ester
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Found 1 products.
Methyl 2-(4-amino-2,6-dichlorophenyl)acetate
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H9Cl2NO2Purity:Min. 95%Molecular weight:234.08 g/mol
