602-03-9

Basic information

• Product Name: 2,3-DINITROANILINE
• Synonyms: 2,3-DINITROANILINE;Aniline, 2,3-dinitro-;Benzenamine, 2,3-dinitro-;(2,3-dinitrophenyl)amine
• CAS NO: 602-03-9
• Molecular Formula: C₆H₅N₃O₄
• Molecular Weight: 183.12
• Mol File: 602-03-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 128°C
• Boiling Point: 316.77°C (rough estimate)
• Flash Point: 210.2 °C
• Appearance: /
• Density: 1.6460
• Refractive Index: 1.6910 (estimate)
• PKA: -2.39±0.10(Predicted)
• CAS DataBase Reference: 2,3-DINITROANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DINITROANILINE(602-03-9)
• EPA Substance Registry System: 2,3-DINITROANILINE(602-03-9)

Safety Data

• Hazardous Substances Data: 602-03-9(Hazardous Substances Data)

Usage

Uses

2,3-Dinitroaniline is a building block used in various chemical synthesis.

Upstream product

• 60956-27-6 N-(2,3-dinitrophenyl)acetamide 
• 7664-93-9 sulfuric acid 
• 62-53-3 aniline 
• 99-09-2 3-nitro-aniline 
• 100663-84-1 ethyl N-(4-acetamido-2-nitrophenyl)carbamate 
• 97-02-9 2,4-Dinitroanilin 
• 57399-97-0 N-(4-aminophenyl)carbamic acid ethyl ester 
• 95182-27-7 ethyl N-(4-acetamidophenyl)carbamate 
• 66-56-8 2,3-dinitrophenol 
• 57-13-6 urea 

Downstream Products

• 608-32-2 1,2,3-triaminobenzene 
• 26429-41-4 1,2-dibromo-3-nitrobenzene 
• 3209-22-1 1,2-Dichloro-3-nitrobenzene 
• 19613-76-4 1-bromo-2,3-dinitro-benzene 
• 619-18-1 2,5-dinitroaniline 
• 610-41-3 3,4-dinitroaniline 
• 51294-42-9 1-iodo-2,3-dinitro-benzene 
• 602-02-8 2,3-dinitrochlorobenzene 
• 116529-43-2 6-bromo-2,3-dinitro-aniline 
• 134293-23-5 2,3,4,6,N-pentanitro-aniline 
• 58538-00-4 2,3,N-trinitro-aniline 
• 528-29-0 1,2-Dinitrobenzene 
• 74628-25-4 2-nitro-5-(1-piperidinyl)aniline 
• 74628-18-5 2-nitro-3-(piperidin-1-yl)aniline 

Relevant articles and documents

1-(ARYLSULFONYL)-4-(PIPERAZIN-1-YL)-1H-BENZIMIDAZOLES AS 5-HYDROXYTRYPTAMINE-6 LIGANDS

The invention relates to 1-(arylsulfonyl)-4-(piperazin-1-yl)-1H-benzimidazole compounds of the Formula I: or a tautomer, stereoisomer, or pharmaceutically acceptable salt thereof, wherein the constituent variables are as defined herein, compositions compr

A Comparison of the Reactions of Some Ethyl N-Arylcarbamates with Those of the Corresponding Acetanilides. I. Nitration

The reactions of some ethyl N-arylcarbamates and of the corresponding acetanilides towards 1 equiv. of sodium nitrate in concentrated sulfuric acid at 0-5 deg have been compared with one another and have been found to exhibit significant differences.Except in the case of the unsubstituted analogues, nitration of the carbamates was found to occur significantly more quickly than that of the acetanilides as shown by (i) a representative competitive nitration, and (ii) the fact the carbamates containing a nitro group are nitrated smoothly whereas the corresponding nitroacetanilides are slow to react.On the basis of competitive reactions, it is suggested that this difference in reactivity is due to steric factors.