CAS 536-90-3
:3-Metoxianilina
- 1-Amino-3-methoxybenzene
- 1-Methoxy-3-aminobenzene
- 3-(Methyloxy)aniline
- 3-Aminoanisole
- 3-Aminophenol methyl ether
- 3-Ethoxyaniline
- 3-Methoxyaniline
- 3-Methoxybenzenamine
- 3-Methoxyphenylamine
- 3-Metoxybenzeneamine
- Anisidine, Meta-
- Benzenamine, 3-methoxy-
- M-Aminoanisole
- M-Anisidina
- Meta anisidine
- Nsc 7631
- m-Aminomethoxybenzene
- m-Anisidin
- m-Anisylamine
- m-Methoxyaniline
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m-Anisidine
CAS:Fórmula:C7H9NOPureza:>98.0%(GC)(T)Forma y color:Colorless to Light orange to Yellow clear liquidPeso molecular:123.16m-Anisidine, 98%
CAS:The unusually large amount of dibromo product produced upon bromination of m-anisidine may be attributed to the two doubly activeated positions. The best enantioselectivity of 97 % ee was observed for the reaction of m-anisidine in organocatalytic asymmetric three-component cyclization of cinnamalde
Fórmula:C7H9NOPureza:98%Forma y color:Liquid, Pale yellow to dark red or dark brownPeso molecular:123.163-Methoxyaniline
CAS:3-MethoxyanilineFórmula:C7H9NOPureza:≥95%Forma y color: very dark red-brown liquidPeso molecular:123.15246g/mol3-Methoxybenzenamine
CAS:3-Methoxybenzenamine is a molecule that can be synthesized by an asymmetric reaction. It has carcinogenic potential and is classified as a chemical substance. 3-Methoxybenzenamine reacts with hydrochloric acid to form hydrogen chloride gas and methoxybenzene. The hydroxyl group on the molecule reacts with l-tartaric acid to form an ester, which then undergoes hydrolysis to produce 3-hydroxybutanoic acid. This reaction also produces water, which may result in a decrease of the concentration of the reactants. 3-Methoxybenzenamine can also react with amines to form quaternary ammonium salts, which are highly soluble in water and have a high detection sensitivity.
Fórmula:C7H9NOPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:123.15 g/mol








