CAS 6921-40-0
:1-Azidonaphthalene
Description:
1-Azidonaphthalene is an organic compound characterized by the presence of an azide functional group (-N3) attached to a naphthalene ring system. It is a yellow to orange solid at room temperature and is known for its aromatic properties, which contribute to its stability and reactivity. The azide group is a notable feature, as it can undergo various chemical transformations, including thermal decomposition and click chemistry reactions, making it useful in synthetic organic chemistry. 1-Azidonaphthalene is typically insoluble in water but may dissolve in organic solvents such as ethanol and acetone. Due to the presence of the azide group, it can be sensitive to heat and shock, necessitating careful handling and storage. This compound is often utilized in research and development, particularly in the fields of materials science and medicinal chemistry, where it can serve as a precursor for the synthesis of more complex molecules. Safety precautions are essential when working with 1-azidonaphthalene due to its potential hazards associated with the azide moiety.
Formula:C10H7N3
InChI:InChI=1/C10H7N3/c11-13-12-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H
InChI key:InChIKey=HYISGPFBRUIUNB-UHFFFAOYSA-N
SMILES:N(=[N+]=[N-])C=1C2=C(C=CC1)C=CC=C2
Synonyms:- 1-Naphthyl azide
- Naphthalene, 1-azido-
- α-Naphthyl azide
- 1-Azidonaphthalene
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1-Azidonaphthalene
CAS:<p>1-Azidonaphthalene is a chemical species that has an absorption band at around 280 nm. It is used in the optical and vibrational spectroscopy of silver trifluoromethanesulfonate, which is a reactive, azide-forming species. The compound can be obtained by reacting 1-naphthol with sodium azide in the presence of cellulose acetate to form a peroxide and an aromatic acid. 1-Azidonaphthalene is unstable due to its intramolecular hydrogen and reacts with oxygen or ozone to generate other chemical species such as nitrosobenzene and nitrobenzene.</p>Formula:C10H7N3Purity:Min. 95%Molecular weight:169.18 g/mol
