50366-20-6

Basic information

• Product Name: N’-(2-hydroxybenzylidene)-4-nitrobenzohydrazide
• Synonyms: N’-(2-hydroxybenzylidene)-4-nitrobenzohydrazide
• CAS NO: 50366-20-6
• Molecular Weight: 285.259
• Mol File: 50366-20-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N’-(2-hydroxybenzylidene)-4-nitrobenzohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N’-(2-hydroxybenzylidene)-4-nitrobenzohydrazide(50366-20-6)
• EPA Substance Registry System: N’-(2-hydroxybenzylidene)-4-nitrobenzohydrazide(50366-20-6)

Safety Data

• Hazardous Substances Data: 50366-20-6(Hazardous Substances Data)

Upstream product

• 99-77-4 ethyl 4-nitrobenzoate 
• 62-23-7 4-nitro-benzoic acid 
• 619-50-1 4-nitrobenzoic acid methyl ester 
• 89-95-2 2-methyl-benzyl alcohol 
• 636-97-5 N-amino-(4-nitrophenyl)carboxamide 
• 90-02-8 salicylaldehyde 

Downstream Products

• 128445-90-9 1,3-Dihydro-1-(4-nitrophenyl)isobenzofuran 
• 1049009-41-7 2-(4-nitrobenzoyl)benzaldehyde 
• 148422-85-9 cobalt(II) 4-nitrobenzoylhydrazone complex 
• 62081-88-3 UO₂⁽²⁺⁾*CH₃COO^(1-)*C₁₄H₁₀N₃O₄^(1-)*H₂O = UO₂(CH₃COO)(C₁₄H₁₀N₃O₄)*H₂O 
• 412351-58-7 [Ge((C₆H₄)OCHN₂CO(C₆H₄(4-NO₂)))2] 

Relevant articles and documents

Tetrabromomethane as an Organic Catalyst: a Kinetic Study of CBr4-Catalyzed Schiff Condensation

Tetrabromomethane functions as an organic catalyst for non-redox reactions of carbonyl species and, in particular, it enhances the aldehyde–acyl hydrazide condensation to give N-acyl hydrazones. This simple, inexpensive, and commercially available halomet

Efficient synthesis of functionalized 1,3-dihydroisobenzofurans from salicylaldehydes: Application to the synthesis of escitalopram

An efficient synthesis of substituted 1,3-dihydroisobenzofurans is developed. In this novel route, o-aroylbenzaldehydes, as key intermediates, can be obtained by lead tetraacetate oxidation of N-aroylhydrazones of salicylaldehydes. The mild and general st

Synthesis of some novel pharmacologically active schiff bases using microwave method and their derivatives formazans by conventional method

Condensation of p-nitrobenzoylhydrazide 1 with substituted aromatic aldehydes 2 under microwave irradiation and by conventional method provide Schiff bases 3a-j. Schiff bases 3a-j on condensation with diazonium salt of 6-methoxy-2-aminobenzothiazole give formazans 4a-j. This reaction is carried out only by conventional method.