CAS 90923-80-1
:4-Amino-2-naphthalenol
Description:
4-Amino-2-naphthalenol, also known as 4-amino-2-naphthol, is an organic compound characterized by the presence of an amino group (-NH2) and a hydroxyl group (-OH) attached to a naphthalene ring system. This compound typically appears as a solid, often with a crystalline structure, and is soluble in polar solvents such as water and alcohols due to its functional groups. It exhibits properties typical of both amines and phenols, including the ability to participate in hydrogen bonding and act as a weak base. The compound is often used in dye synthesis, particularly in the production of azo dyes, and may also serve as an intermediate in organic synthesis. Additionally, 4-amino-2-naphthalenol can exhibit biological activity, making it of interest in pharmaceutical research. Safety considerations should be taken into account when handling this compound, as it may pose health risks if ingested or inhaled. Proper laboratory practices and personal protective equipment are recommended when working with this substance.
Formula:C10H9NO
InChI:InChI=1S/C10H9NO/c11-10-6-8(12)5-7-3-1-2-4-9(7)10/h1-6,12H,11H2
InChI key:InChIKey=HZVWUBNSJFILOV-UHFFFAOYSA-N
SMILES:NC=1C2=C(C=C(O)C1)C=CC=C2
Synonyms:- 3-Hydroxy-1-naphthylamine
- 2-Naphthol, 4-amino-
- 4-Amino-2-naphthol
- 4-Amino-2-naphthalenol
- 2-Naphthalenol, 4-amino-
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Found 4 products.
4-Aminonaphthalen-2-ol
CAS:<p>4-Aminonaphthalen-2-ol is a synthetic reagent that is used in organic chemistry. It can be prepared from the reaction of chlorides and benzofurans, which are synthesized from an electrophilic aromatic substitution reaction with sodium hydroxide. The efficiency of this process can be enhanced by using imidazole as a solvent or as a catalyst for the reaction. 4-Aminonaphthalen-2-ol is also used in the synthesis of imidazole derivatives, such as 2-(4-aminophenyl)imidazo[1,2-a]pyridine.</p>Formula:C10H9NOPurity:Min. 95%Molecular weight:159.18 g/mol
