CAS 35613-44-6
:Methyl 2-aminobenzeneacetate
Description:
Methyl 2-aminobenzeneacetate, also known as methyl o-aminobenzoate, is an organic compound characterized by its ester functional group derived from the reaction of 2-aminobenzoic acid and methanol. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. This compound features an aromatic ring, which contributes to its stability and potential reactivity. Methyl 2-aminobenzeneacetate is soluble in organic solvents such as ethanol and ether, but its solubility in water is limited due to the hydrophobic nature of the aromatic ring. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, agrochemicals, and dyes. The presence of the amino group can impart basic properties, allowing it to participate in various chemical reactions, including acylation and alkylation. As with many organic compounds, safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled.
Formula:C9H11NO2
InChI:InChI=1S/C9H11NO2/c1-12-9(11)6-7-4-2-3-5-8(7)10/h2-5H,6,10H2,1H3
InChI key:InChIKey=BWQBYHGDMBHIIQ-UHFFFAOYSA-N
SMILES:C(C(OC)=O)C1=C(N)C=CC=C1
Synonyms:- (2-Aminophenyl)acetic acid methyl ester
- 2-Aminohydratropic acid
- Acetic acid, (o-aminophenyl)-, methyl ester
- Benzeneacetic Acid, 2-Amino-Alpha-Methyl-
- Benzeneacetic acid, 2-amino-, methyl ester
- Methyl 2-aminobenzeneacetate
- Methyl 2-aminophenylacetate
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Found 4 products.
Methyl (2-amino-phenyl)-acetate
CAS:Formula:C9H11NO2Purity:95%Color and Shape:LiquidMolecular weight:165.1891Methyl (2-amino-phenyl)acetate
CAS:Methyl (2-amino-phenyl)acetateFormula:C9H11NO2Purity:96%Color and Shape: pale yellow liquidMolecular weight:165.19g/molMethyl 2-(2-aminophenyl)acetate
CAS:Formula:C9H11NO2Purity:97%Color and Shape:LiquidMolecular weight:165.192Methyl 2-(2-aminophenyl)acetate
CAS:<p>Methyl 2-(2-aminophenyl)acetate is a synthetic compound that can be activated with nanomolar concentrations of cyanide. It is a potent cytotoxic agent that exhibits minimal activity in the presence of cells. Methyl 2-(2-aminophenyl)acetate has shown to have antiviral and antitumor properties, as well as potential use in cancer therapy. Methyl 2-(2-aminophenyl)acetate is synthesized by reacting an aldehyde group with a primary amine to produce an amide bond. This reaction also produces a linker molecule, which can be used for immobilization. Immobilization occurs when the chemical is bound to an insoluble support or carrier, such as silica gel or glass beads. Immobilization can increase the stability of the reactant, decrease its rate of degradation, and facilitate separation from unreacted components.</p>Formula:C9H11NO2Purity:Min. 95%Molecular weight:165.19 g/mol



