CAS 31499-54-4
:Benzenemethanol, 4-azido-
Description:
Benzenemethanol, 4-azido- is an organic compound characterized by the presence of both a benzene ring and an azido group (-N3) attached to a methanol moiety. This compound typically exhibits a white to light yellow crystalline appearance and is soluble in organic solvents. The azido group is known for its reactivity, particularly in click chemistry and as a precursor for various nitrogen-containing compounds. The presence of the hydroxymethyl group (-CH2OH) contributes to its potential as a building block in organic synthesis. Additionally, the compound may exhibit moderate to low toxicity, necessitating careful handling and storage. Its unique functional groups allow for various chemical transformations, making it of interest in both academic research and industrial applications, particularly in the fields of materials science and medicinal chemistry. As with many azido compounds, it is important to consider stability and safety precautions due to the potential for explosive decomposition under certain conditions.
Formula:C7H7N3O
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Found 4 products.
(4-Azidophenyl)methanol
CAS:Controlled ProductFormula:C7H8N3OColor and Shape:NeatMolecular weight:150.158(4-Azidophenyl)methanol
CAS:<p>4-Azidophenylmethanol is a nucleophilic amine that can be synthesized from the reaction of an azide with a methoxide. 4-Azidophenylmethanol can be used to generate nitro groups in organic synthesis. It has also been shown to have cytotoxic activity against prostate cancer cells and malignant brain cancer. 4-Azidophenylmethanol also has the ability to react with squamous carcinoma cells, forming methides and causing cell death. This chemical is stable at low temperatures and does not react with water.</p>Formula:C7H7N3OPurity:Min. 95%Color and Shape:PowderMolecular weight:149.15 g/mol4-Azidobenzyl alcohol
CAS:<p>4-Azidobenzyl alcohol is a click chemistry reagent containing an azide group.</p>Formula:C7H7N3OPurity:99.937%Color and Shape:SolidMolecular weight:149.15



