CAS 29091-40-5

2,1,3-Benzoxadiazole, 4-methyl-

Description:

2,1,3-Benzoxadiazole, 4-methyl- is an organic compound characterized by its bicyclic structure, which consists of a benzene ring fused to a benzodiazole moiety. This compound features a methyl group at the 4-position of the benzodiazole ring, influencing its chemical properties and reactivity. It is typically a solid at room temperature and exhibits moderate solubility in organic solvents. The presence of the benzoxadiazole structure imparts notable fluorescence properties, making it of interest in various applications, including organic light-emitting diodes (OLEDs) and fluorescent probes in biological systems. Additionally, it may exhibit biological activity, which can be explored for potential pharmaceutical applications. The compound's stability and reactivity can be influenced by the substituents on the benzodiazole ring, and it may undergo various chemical reactions typical of aromatic compounds, such as electrophilic substitution. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₇H₆N₂O

Synonyms:

• Benzofurazan, 4-methyl-
• 4-Methylbenzofurazan

2,1,3-Benzoxadiazole, 4-methyl-

CAS: 29091-40-5

Formula: C₇H₆N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 134.1353

Ref: IN-DA002XAU

4-methyl-2,1,3-benzoxadiazole

CAS: 29091-40-5

4-methyl-2,1,3-benzoxadiazole

Purity: 95%

Molecular weight: 134.14g/mol

Ref: 54-OR21980

4-Methyl-2,1,3-benzoxadiazole

CAS: 29091-40-5

4-Methyl-2,1,3-benzoxadiazole is a hexamethylenetetramine derivative that is used as an excipient in pharmaceuticals. It has been shown to have high yield and good solubility properties. 4-Methyl-2,1,3-benzoxadiazole can be hydrolyzed by acidolysis to form the corresponding carboxylic acid. The optimal reaction time for this process is between 5 and 10 minutes at room temperature. The product of this reaction can be purified by boiling with water or cooled with ether. 4-Methyl-2,1,3-benzoxadiazole can react with bromosuccinimide to form the corresponding bromohydrin derivative in a peroxide reaction. The optimal reaction time for this process is between 2 and 3 hours at room temperature. Hydrolysis of the bromohydrin yields the corresponding alcohol. This product can

Formula: C₇H₆N₂O

Purity: Min. 95%

Molecular weight: 134.14 g/mol

Ref: 3D-EBA09140