51348-06-2

Basic information

• Product Name: N-hydroxy-2,4-dinitroaniline
• Synonyms: Benzenamine, N-hydroxy-2,4-dinitro-; N-Hydroxy-2,4-dinitrobenzenamine
• CAS NO: 51348-06-2
• Molecular Formula: C₆H₅N₃O₅
• Molecular Weight: 199.121
• Mol File: 51348-06-2.mol

Chemical Properties

• Boiling Point: 391°C at 760 mmHg
• Flash Point: 190.3°C
• Density: 1.753g/cm³
• Vapor Pressure: 8.14E-07mmHg at 25°C
• Refractive Index: 1.741
• CAS DataBase Reference: N-hydroxy-2,4-dinitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-hydroxy-2,4-dinitroaniline(51348-06-2)
• EPA Substance Registry System: N-hydroxy-2,4-dinitroaniline(51348-06-2)

Safety Data

• Hazardous Substances Data: 51348-06-2(Hazardous Substances Data)

Upstream product

• 119-27-7 2,4-dinitroanisole 
• 7803-49-8 hydroxylamine 
• 141-52-6 sodium ethanolate 
• 2486-07-9 2,4-dinitrophenyl phenyl ether 
• 70-34-8 2,4-Dinitrofluorobenzene 

Downstream Products

• 98555-19-2 N-acetoxy-2,4-dinitrobenzenamine 
• 18771-86-3 5-nitrobenzofuroxan 
• 97-02-9 2,4-Dinitroanilin 
• 127553-53-1 N-(4'-nitrobenzoyloxy)-2,4-dinitrobenzenamine 
• 610-31-1 1,2,4-trinitrobenzene 
• 388069-27-0 (6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-ylmethyl)-(2,4-dinitro-phenyl)-amine 
• 388069-25-8 (2,4-dinitro-phenyl)-(2-phenyl-allyl)-amine 
• 28943-91-1 2,2',4,4'-tetranitroazoxybenzene 
• 961-68-2 N-phenyl-2,4-dinitroaniline 
• 51348-04-0 N,O-dimethyl-N-(2,4-dinitro-phenyl)-hydroxylamine 
• 110319-05-6 N-acetoxy-N-acetyl-2,4-dinitrophenylamine 
• 388069-23-6 (2,4-dinitro-phenyl)-(1-ethyl-2-methyl-allyl)-amine 
• 110319-04-5 N-hydroxy-N-acetyl-2,4-dinitrophenylamine 
• 388069-37-2 (6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-ylmethyl)-(2,4-dinitro-phenyl)-methyl-amine 

Relevant articles and documents

2,4-Dinitrophenylhydroxylamine: An efficient and more general reagent for iron-catalyzed allylic amination

2,4-Dinitrophenylhydroxylamine (1) is an efficient reagent for the iron-catalyzed regioselective allylic amination of olefins. Moderate to excellent yields of N-DNP-N-allyl amines (2) are obtained resulting from introduction of the N-DNP group at the less

A STUDY OF NUCLEOPHILICITY IN SELECTED SYSTEMS

Kinetic studies have been carried out of the reactions of 15 nucleophiles with 2,4-dinitrophenyl acetate and 14 nucleophiles with 2,4-dinitrofluorobenzene in 52percent (w/w) methanol at 25 deg C.The rate constant values obtained and literature data have been treated by the factor analysis.It has been found that the description of nucleophilicity at least needs two factors.The nucleophiles studied are divided into two groups (ionic and nitrogen-containing ones).In each group, the nucleophilic properties are affected by linear combination of both factors.