92166-40-0

Basic information

• Product Name: N-[2-(hydrazinylcarbonyl)phenyl]benzamide
• Synonyms: benzoic acid, 2-(benzoylamino)-, hydrazide; N-[2-(Hydrazinocarbonyl)phenyl]benzamide
• CAS NO: 92166-40-0
• Molecular Formula: C₁₄H₁₃N₃O₂
• Molecular Weight: 255.2719
• Mol File: 92166-40-0.mol
• Article Data: 10

Chemical Properties

• Density: 1.303g/cm³
• Refractive Index: 1.672
• CAS DataBase Reference: N-[2-(hydrazinylcarbonyl)phenyl]benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(hydrazinylcarbonyl)phenyl]benzamide(92166-40-0)
• EPA Substance Registry System: N-[2-(hydrazinylcarbonyl)phenyl]benzamide(92166-40-0)

Safety Data

• Hazardous Substances Data: 92166-40-0(Hazardous Substances Data)

Upstream product

• 1022-46-4 2-phenyl-4H-3,1-benzoxazin-4-one 
• 7510-49-8 methyl 2-(benzamido)benzoate 
• 64-17-5 ethanol 
• 7803-57-8 hydrazine hydrate 
• 1904-60-5 3-amino-2-phenylquinazolin-4(3H)-one 
• 98-88-4 benzoyl chloride 
• 134-20-3 2-carbomethoxyaniline 
• 118-92-3 anthranilic acid 
• 579-93-1 2-(Benzoylamino)benzoic Acid 
• 42091-29-2 4-ethoxy-1H-2,1-benzothiazine 2,2-dioxide 
• 65-85-0 benzoic acid 

Downstream Products

• 1904-60-5 3-amino-2-phenylquinazolin-4(3H)-one 
• 139435-26-0 2-(o-benzoylaminophenyl)-1,3,4-oxadiazolin-5-thione 
• 139435-27-1 N-[2-(5-Ethylsulfanyl-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide 
• 139435-29-3 C₁₉H₂₂N₄O₂S 
• 139435-30-6 N-[2-(5-Morpholin-4-yl-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide 
• 139435-31-7 C₂₂H₂₀N₄O₂S 
• 139435-28-2 N-[2-(4-Morpholin-4-ylmethyl-5-thioxo-4,5-dihydro-[1,3,4]oxadiazol-2-yl)-phenyl]-benzamide 
• 97625-15-5 3-Diacetylamino-2-phenyl-4(3H)-quinazolinone 
• 939967-84-7 N-(2-{[(2E)-2-(2-hydroxybenzylidene)hydrazinyl]carbonyl}phenyl)benzamide 

Relevant articles and documents

Aluminum ion detection fluorescent probe based on bifunctional organic small molecule as matrix and preparation method and application thereof

The invention discloses an aluminum ion detection fluorescent probe based on a bifunctional organic small molecule as a matrix and a preparation method and application of the fluorescence probe, and the structural formula is shown I. To the invention, 1, 8 - naphthalimide and isoquinoline hydrazide or 2 - benzamide benzoyl hydrazine are used as fluorescent groups, and the prepared Schiff base type probe NIQ or NBP is prepared into a solution Al through condensation reaction. 3 + High sensitivity and high selectivity are exhibited, and at the same time, the structure is stable. The low toxicity and cell infiltration capability is strong, and the trace metal aluminum ions in the living Hela cells are successfully detected. The preparation method of the fluorescent probe is simple, the raw materials are easily available, the obtained product is solid powder, is easy to store, and has a high application development prospect.

A highly selective diarylethene fluorescence sensor of aluminum ion and its application

A novel diarylethene derivative 1O with the unit of N-(2-(hydrazinecarbonyl)phenyl)benzamide was designed and synthesized successfully. The sensor showed excellent photochromism and specific fluorescent detection toward aluminum ion with rarely interfering. The emission intensity could increase nearly by 100 folds with aluminum ion and the color changed from dark to Aqua green. The low limit of detection (LOD) of 1O was determined as 3.26 × 10-8 mol L-1. Additionally, the sensor could be used in logic circuit and aluminum ion detection in untreated water.

A new series of Schiff base derivatives bearing 1,2,3-triazole: Design, synthesis, molecular docking, and α-glucosidase inhibition

A series of new Schiff bases bearing 1,2,3-triazole 12a?o was designed, synthesized, and evaluated as α-glucosidase inhibitors. All the synthesized compounds showed promising inhibition against α-glucosidase and were more potent than the standard drug aca