3078-09-9

Basic information

• Product Name: BENZALDEHYDE 4-NITROPHENYLHYDRAZONE
• Synonyms: BENZALDEHYDE P-NITROPHENYL-HYDRAZONE;BENZALDEHYDE 4-NITROPHENYLHYDRAZONE;BENZAL-4-NITROPHENYLHYDRAZONE;BENZALDEHYDE 4-NITROPHENYLHYDRAZONE 98%;Benzaldehyde, (p-nitrophenyl)hydrazone (8ci);Benzaldehyde, 2-(4-nitrophenyl)hydrazone;Nsc 85453
• CAS NO: 3078-09-9
• Molecular Formula: C₁₃H₁₁N₃O₂
• Molecular Weight: 241.25
• Product Categories: Hydrazones;Nitrogen Compounds;Organic Building Blocks
• Mol File: 3078-09-9.mol
• Article Data: 8

Chemical Properties

• Melting Point: 193.0 to 197.0 °C
• Boiling Point: 410.4°Cat760mmHg
• Flash Point: 202°C
• Appearance: /
• Density: 1.2g/cm³
• Vapor Pressure: 6.06E-07mmHg at 25°C
• Refractive Index: 1.608
• Storage Temp.: 2-8°C
• PKA: 12.38±0.10(Predicted)
• CAS DataBase Reference: BENZALDEHYDE 4-NITROPHENYLHYDRAZONE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZALDEHYDE 4-NITROPHENYLHYDRAZONE(3078-09-9)
• EPA Substance Registry System: BENZALDEHYDE 4-NITROPHENYLHYDRAZONE(3078-09-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 3078-09-9(Hazardous Substances Data)

Usage

General Description

Benzaldehyde 4-nitrophenylhydrazone is a chemical compound derived from benzaldehyde and hydrazine, which has a molecular formula of C13H10N4O2. It is commonly used as a reagent in organic chemistry for the detection and quantification of aldehydes and ketones. The compound is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. It is also used as a building block for the synthesis of various pharmaceutical and agrochemical compounds. Additionally, benzaldehyde 4-nitrophenylhydrazone has been studied for its potential antitumor and antibacterial properties.

InChI:InChI=1/C13H11N3O2/c17-16(18)13-8-6-12(7-9-13)15-14-10-11-4-2-1-3-5-11/h1-10,15H/b14-10+

Upstream product

• 100-16-3 4-nitrophenylhydrazone 
• 622-79-7 benzyl azide 
• 141-52-6 sodium ethanolate 
• 64-17-5 ethanol 
• 588-64-7 benzaldehyde phenylhydrazone 
• 71-43-2 benzene 
• 100-44-7 benzyl chloride 
• 56-23-5 tetrachloromethane 
• 100-52-7 benzaldehyde 

Downstream Products

• 33356-51-3 acetic acid-[benzylidene-(4-nitro-phenyl)-hydrazide] 
• 14947-42-3 benzaldehyde-[methyl-(4-nitro-phenyl)-hydrazone] 
• 13443-96-4 N-benzoyl-N'-(4-nitrophenyl)diazene 
• 100-52-7 benzaldehyde 
• 1370004-47-9 C₁₇H₁₆N₄O₂ 
• 65-85-0 benzoic acid 
• 26631-44-7 1-p-nitrophenyl-3-phenyl-5-cyano-4,5-dihydro-2-pyrazoline 
• 4702-72-1 benzil mono(p-nitrophenylhydrazone) 
• 962-13-0 N-(4-nitrophenyl)benzohydrazonoyl bromide 
• 77721-75-6 (α-nitro-benzylidene)-(4-nitro-phenyl)-hydrazine 
• 115591-25-8 5-ethyl-1-(4-nitrophenyl)-3-phenyl-1,2,4-triazole 
• 88246-21-3 (4-Nitro-phenyl)-[phenyl-(4,5,6,7-tetrahydro-benzo[1,3]dithiol-2-ylidene)-methyl]-diazene 
• 79708-14-8 C₂₁H₂₀N₆O₂ 
• 16580-57-7 1,3-diphenyl-5-(4-nitrophenyl)formazan 

Relevant articles and documents

Synthesis and evaluation of anti-Tuberculosis and anti-cancer activities of hydrazones and N-Acylhydrazones by using sonochemistry, a new general procedure

Background: In continuation of our research on sonochemistry and due to the importance and application of hydrazones and N-Acylhydrazones in drug discovery, in this work we report a new general and efficient synthesis of these classes with different aromatic and heteroaromatic nucleus assisted by ultrasound and their respective anti-Tuberculosis and anti-cancer activities. Method: Derivatives 7-chloroquinoline 10 and 12 were the most promising compounds against cancer and TB, respectively. Conclusion: Unfortunately all new hydrazones and N-Acylhydrazones evaluated displayed no activity anti cancer and TB.

TETRAZOLIUM COMPOUND FOR DETECTING MICROORGANISMS, REAGENT FOR DETECTING MICROORGANISMS AND METHOD FOR DETECTING MICROORGANISMS

The object of the present invention is to provide a compound used in a reagent for detecting microorganisms, by which microorganisms can be rapidly and reliably detected without requiring any special instrument, the reagent for detecting microorganisms, a

Ultrasound assisted syntheses of some 1,2,4-triazole derivatives

A facile preparation of a series of 1,2,4-triazole derivatives under ultrasound irradiation, that proceeded via one-pot reaction of a- nitrophenyl hydrazones with different methylene amines, using sodium nitrite as oxidant and benzyl triethyl ammonium chloride (BTEAC) as phase transfer catalysis, respectively, was described.