CAS 850364-08-8

1H-Indazole,4-(phenylmethoxy)-

Description:

1H-Indazole, 4-(phenylmethoxy)- is an organic compound characterized by its indazole core, which consists of a five-membered ring containing two nitrogen atoms. The presence of a phenylmethoxy group at the 4-position of the indazole structure enhances its chemical properties, potentially influencing its reactivity and solubility. This compound may exhibit various biological activities, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential interactions with biological targets, which could be explored for therapeutic applications. The compound is likely to be a solid at room temperature and may have moderate to low solubility in water, typical of many indazole derivatives. Additionally, it may undergo typical organic reactions such as substitution or oxidation, depending on the functional groups present. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity. Overall, 1H-Indazole, 4-(phenylmethoxy)- represents a class of compounds that could be valuable in research and pharmaceutical contexts.

Formula: C₁₄H₁₂N₂O

Synonyms:

• 4-Benzyloxy-1H-indazole

4-(benzyloxy)-1H-indazole

CAS: 850364-08-8

Formula: C₁₄H₁₂N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 224.2579

Ref: IN-DA003KT3

4-(Benzyloxy)-1H-indazole

CAS: 850364-08-8

4-(Benzyloxy)-1H-indazole

Purity: 95%

Molecular weight: 223.25g/mol

Ref: 54-OR1004630

4-(Benzyloxy)-1H-indazole

CAS: 850364-08-8

Purity: 95.0%

Molecular weight: 224.26300048828125

Ref: 10-F224523

4-(Benzyloxy)-1H-indazole

CAS: 850364-08-8

4-(Benzyloxy)-1H-indazole is a chemical compound that is synthesized by the reaction of 4-hydroxy-1H-indazole with benzyl bromide. This reaction proceeds through two steps: 1) diazotization and 2) aminolysis. The isoamyl acetate produced in step 1 reacts with the indazole in step 2 to produce 4-(benzyloxy)-1H-indazole. The reaction temperature for this process should be kept at or below 40°C, as it can result in a low yield of product. This chemical compound has been used as a nucleophile in various reactions and has been shown to react with nitrite ions to form an azine derivative.

Formula: C₁₄H₁₂N₂O

Purity: Min. 95%

Molecular weight: 224.26 g/mol

Ref: 3D-AJB36408