145260-32-8

Basic information

• Product Name: N'-[(E)-(2-METHOXYPHENYL)METHYLIDENE]BENZENESULFONOHYDRAZIDE
• Synonyms: N'-[(E)-(2-METHOXYPHENYL)METHYLIDENE]BENZENESULFONOHYDRAZIDE;N'-[(1E)-(2-methoxyphenyl)methylidene]benzenesulfonohydrazide
• CAS NO: 145260-32-8
• Molecular Formula: C₁₄H₁₄N₂O₃S
• Molecular Weight: 290.34
• Mol File: 145260-32-8.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N'-[(E)-(2-METHOXYPHENYL)METHYLIDENE]BENZENESULFONOHYDRAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N'-[(E)-(2-METHOXYPHENYL)METHYLIDENE]BENZENESULFONOHYDRAZIDE(145260-32-8)
• EPA Substance Registry System: N'-[(E)-(2-METHOXYPHENYL)METHYLIDENE]BENZENESULFONOHYDRAZIDE(145260-32-8)

Safety Data

• Hazardous Substances Data: 145260-32-8(Hazardous Substances Data)

Usage

General Description

(E)-N'-(2-methoxybenzylidene)benzenesulfonohydrazide is a chemical compound with a molecular formula C14H13N3O3S. It is a hydrazide derivative of benzenesulfonohydrazide and has a molecular mass of 303.34 g/mol. (E)-N'-(2-methoxybenzylidene)benzenesulfonohydrazide has potential applications in the pharmaceutical and chemical industries, where it can be used as a reagent in organic synthesis and in the development of new drugs. It may also possess biological activities and could be further investigated for its potential therapeutic properties. Additionally, its unique structure and properties make it a candidate for research in the development of advanced materials and specialty chemicals.

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 80-17-1 benzenesufonyl hydrazide 

Downstream Products

• 737733-33-4 2,5-bis(2-methoxyphenyl)-2H-tetrazole 
• 1262442-56-7 2,5-bis(o-phenolyl)tetrazole 
• 1262442-72-7 3-(1,3-bis(2-methoxyphenyl)-4,5-dihydro-1H-pyrazol-5-yl)propan-1-ol 

Relevant articles and documents

Fabrication of a Ga3+ sensor probe based on methoxybenzylidenebenzenesulfonohydrazide (MBBSH) by an electrochemical approach

A series of (E)-N′-methoxybenzylidene-benzenesulfonohydrazide (MBBSH) compounds were synthesized using a condensation method from the derivatives of methoxybenzaldehyde and benzenesulfonylhydrazine in good (crystallized) yield in an alcoholic medium. The as-prepared MBBSH compounds were well-characterized using various spectroscopic techniques, such as 1H-NMR, 13C-NMR, FTIR, and UV-Vis. The structure of the MBBSH molecules was confirmed using the single crystal X-ray diffraction (SCXRD) method and used for the selective detection of the gallium (Ga3+) ion by the I-V technique. A thin-layer of MBBSH was prepared by deposition onto a smooth glassy carbon electrode (GCE) with Nafion (Nf) as a coating binder in order to modify the sensitive and selective Ga3+ sensor probe. The sensitivity, the limit of detection (LOD), and the limit of quantification (LOQ) of the modified electrode towards Ga3+ were calculated from the calibration curve as 949.37 pA μM-1 cm-2, ≈84.0 ± 0.2 pM, and 280.0 ± 0.5 mM, respectively. The prospective MBBSH/GCE sensor was applied for the determination of Ga3+ in spiked biological (human, mouse, and rabbit serum) and environmental (industrial effluent, red sea water, well-water, and tap water) samples and acceptable and reasonable results were obtained.