CAS 2246-42-6
:2-Methoxy-1-naphthalenamine
Description:
2-Methoxy-1-naphthalenamine, with the CAS number 2246-42-6, is an organic compound characterized by its naphthalene structure substituted with a methoxy group and an amino group. This compound typically appears as a solid or liquid, depending on its purity and specific conditions. It is known for its aromatic properties, which contribute to its potential applications in various fields, including organic synthesis and materials science. The presence of the methoxy group enhances its solubility in organic solvents, while the amino group can participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions. Additionally, 2-methoxy-1-naphthalenamine may exhibit biological activity, making it of interest in medicinal chemistry. Its stability and reactivity can be influenced by environmental factors such as pH and temperature. Safety data sheets should be consulted for handling and storage guidelines, as with any chemical substance, to ensure safe laboratory practices.
Formula:C11H11NO
InChI:InChI=1S/C11H11NO/c1-13-10-7-6-8-4-2-3-5-9(8)11(10)12/h2-7H,12H2,1H3
InChI key:InChIKey=FAOJNWOJCPKVTM-UHFFFAOYSA-N
SMILES:NC=1C2=C(C=CC1OC)C=CC=C2
Synonyms:- 2-Methoxy-1-naphthalenamine
- 1-Naphthylamine, 2-methoxy-
- 1-Amino-2-methoxynaphthalene
- 2-Methoxynaphthalen-1-amine
- 2-Methoxy-1-naphthylamine
- 1-Naphthalenamine, 2-methoxy-
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Found 4 products.
1-Naphthalenamine,2-methoxy-
CAS:Formula:C11H11NOPurity:97%Color and Shape:SolidMolecular weight:173.21112-Methoxynaphthalen-1-amine
CAS:<p>2-Methoxynaphthalen-1-amine</p>Purity:99%Molecular weight:173.21g/mol2-Methoxynaphthalen-1-amine
CAS:<p>2-Methoxynaphthalen-1-amine is a sulphonic acid derivative of naphthalene that can be found in the blood as a result of exposure to this chemical. It has been used in the past for medicinal purposes, and is now known to have potential use as an inhibitor of Alzheimer's disease. 2-Methoxynaphthalen-1-amine is a ternary compound containing three different functional groups; two methoxy groups, one phenyl group and one amine group. The presence of these functional groups gives it the ability to bind with sulphonic acids, which are often found in brain tissue. This bond between 2-methoxynaphthalen-1-amine and sulphonic acids may contribute to its inhibitory effects on Alzheimer's disease by preventing the formation of beta amyloid plaques.</p>Formula:C11H11NOPurity:Min. 95%Molecular weight:173.21 g/mol



