CAS 128958-65-6

4-Benzyloxybenzohydrazide

Description:

4-Benzyloxybenzohydrazide is an organic compound characterized by its hydrazide functional group, which is linked to a benzene ring substituted with a benzyloxy group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide, but may have limited solubility in water. Its molecular structure features a hydrazide moiety, which can participate in various chemical reactions, making it useful in synthetic organic chemistry. The presence of the benzyloxy group enhances its stability and can influence its reactivity, potentially allowing for applications in pharmaceuticals or as intermediates in organic synthesis. Additionally, compounds like 4-Benzyloxybenzohydrazide may exhibit biological activity, which warrants further investigation for potential therapeutic uses. As with many organic compounds, safety precautions should be taken when handling it, including the use of appropriate personal protective equipment and adherence to safety data sheet guidelines.

Formula: C₁₄H₁₄N₂O₂

InChI: InChI=1/C14H14N2O2/c15-16-14(17)12-6-8-13(9-7-12)18-10-11-4-2-1-3-5-11/h1-9H,10,15H2,(H,16,17)

SMILES: c1ccc(cc1)COc1ccc(cc1)C(=O)NN

Synonyms:

• 4-Benzyloxybenzhydrazide
• 4-Benzyloxybenzoic Acid Hydrazide
• Akos Bbb/184
• 4-Benzyloxybenzhydrazide 98%

Benzoic acid, 4-(phenylmethoxy)-, hydrazide

CAS: 128958-65-6

Formula: C₁₄H₁₄N₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 242.2732

Ref: IN-DA000YPN

4-Benzyloxybenzhydrazide

CAS: 128958-65-6

4-Benzyloxybenzhydrazide

Purity: 97%

Molecular weight: 242.27316g/mol

Ref: 54-OR6542

4-Benzyloxybenzhydrazide

CAS: 128958-65-6

Formula: C₁₄H₁₄N₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 242.278

Ref: 10-F018218

4-(Benzyloxy)benzohydrazide

CAS: 128958-65-6

4-(Benzyloxy)benzohydrazide is a new, potent and selective inhibitor of candida glabrata and cryptococcus neoformans. It has been shown to inhibit the growth of cancer cells in vitro and can be used to rationalize the anticancer properties of formamide. This compound inhibits chloride ion uptake in tuberculosis bacteria, which may be responsible for its antifungal activity. 4-(Benzyloxy)benzohydrazide has been synthesized by reacting benzaldehyde with hydrazine hydrate in the presence of a base, such as sodium bicarbonate or potassium carbonate. The reaction occurs at temperatures between room temperature and 120°C. The product is purified by recrystallization from water or acetone, or by column chromatography on silica gel using chloroform-methanol (1:1) as eluent.

Formula: C₁₄H₁₄N₂O₂

Purity: Min. 95%

Molecular weight: 242.27 g/mol

Ref: 3D-DFA95865