CAS 3378-82-3
:1-Bromo-2-naphthalenecarboxaldehyde
Description:
1-Bromo-2-naphthalenecarboxaldehyde is an organic compound characterized by its structure, which features a naphthalene ring substituted with a bromine atom and an aldehyde functional group. This compound is typically a pale yellow to brown solid at room temperature and is known for its aromatic properties due to the presence of the naphthalene moiety. It has a relatively high melting point and is soluble in organic solvents such as dichloromethane and ethanol, but less soluble in water. The bromine substituent enhances its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the aldehyde group allows for further functionalization, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Safety considerations should be taken into account when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate protective measures should be employed.
Formula:C11H7BrO
InChI:InChI=1S/C11H7BrO/c12-11-9(7-13)6-5-8-3-1-2-4-10(8)11/h1-7H
InChI key:InChIKey=CYGUXEZVBLMVRV-UHFFFAOYSA-N
SMILES:BrC=1C2=C(C=CC1C=O)C=CC=C2
Synonyms:- 1-Bromo-2-naphthaldehyde
- 1-Bromo-2-naphthalenecarboxaldehyde
- 1-Bromonaphthalene-2-Carbaldehyde
- 2-Naphthaldehyde, 1-bromo-
- 2-Naphthalenecarboxaldehyde, 1-bromo-
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Found 6 products.
1-Bromo-2-naphthaldehyde
CAS:Formula:C11H7BrOPurity:>96.0%(GC)Color and Shape:White - Yellow Solid FormMolecular weight:235.081-BROMO-2-NAPHTHALDEHYDE
CAS:Formula:C11H7BrOPurity:95%Color and Shape:SolidMolecular weight:235.07671-Bromo-2-naphthaldehyde
CAS:Controlled ProductFormula:C11H7BrOColor and Shape:NeatMolecular weight:235.081-Bromo-2-naphthaldehyde
CAS:<p>1-Bromo-2-naphthaldehyde is a reactive aldehyde that reacts with alkyl halides to form unsymmetrical adducts. This compound undergoes intramolecular hydrogenation and can be used as an excellent starting material for synthesizing ferrocenes. 1-Bromo-2-naphthaldehyde is also used in the synthesis of photochromic compounds, which are compounds that change color when exposed to ultraviolet radiation. 1-Bromo-2-naphthaldehyde undergoes protonation and forms hydrogen bonds with other molecules, making it useful for research on hydrogen bonding.</p>Formula:C11H7BrOPurity:Min. 95%Molecular weight:235.08 g/mol





