69951-03-7

Basic information

• Product Name: BENZENAMINE, 2,3-DICHLORO-4-NITRO-
• Synonyms: BENZENAMINE, 2,3-DICHLORO-4-NITRO-;2-Fluoro-3-methoxyphenylboronicacidBrassfoil
• CAS NO: 69951-03-7
• Molecular Formula: C₆H₄Cl₂N₂O₂
• Molecular Weight: 207.01
• Mol File: 69951-03-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 367.4±37.0 °C(Predicted)
• Appearance: /
• Density: 1.624±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: -2.10±0.14(Predicted)
• CAS DataBase Reference: BENZENAMINE, 2,3-DICHLORO-4-NITRO-(CAS DataBase Reference)
• NIST Chemistry Reference: BENZENAMINE, 2,3-DICHLORO-4-NITRO-(69951-03-7)
• EPA Substance Registry System: BENZENAMINE, 2,3-DICHLORO-4-NITRO-(69951-03-7)

Safety Data

• Hazardous Substances Data: 69951-03-7(Hazardous Substances Data)

Usage

General Description

Benzenamine, 2,3-dichloro-4-nitro- is a chemical compound with the molecular formula C6H3Cl2N2O2. It is a dark yellow to brown solid at room temperature and is mainly used in the manufacture of dyes, pigments, and pharmaceuticals. Benzenamine, 2,3-dichloro-4-nitro- is known to be toxic if ingested, inhaled, or absorbed through skin contact. It is also a suspected human carcinogen and is classified as a hazardous substance by various regulatory agencies. In addition, it is known to be harmful to aquatic life and is listed as a priority pollutant. Overall, Benzenamine, 2,3-dichloro-4-nitro- should be handled with caution and proper safety measures should be taken when working with this substance.

Upstream product

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Downstream Products

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Relevant articles and documents

Design, synthesis, and preliminary in vitro and in silico antiviral activity of [4,7]phenantrolines and 1-oxo-1,4-dihydro-[4,7]phenantrolines against single-stranded positive-sense RNA genome viruses

Following the antiviral screening of a wide series of new angular and linear N-tricyclic systems both in silico and in vitro, the [4,7]phenantroline nucleus emerged as a new ring system endowed with activity against viruses containing single-stranded, positive-sense RNA genomes (ssRNA+). Here, we report our new pathway to the synthesis of this nucleus and of several related derivatives, as well as the results of both cell-based antiviral assays and molecular dynamics simulations. In the antiviral screening, several compounds (9 and 16-20) showed to be fairly active against BVDV, CVB-2, and Polio 1 (EC50, 6-25 μM). According to molecular dynamics simulations, compounds (15) and (17) emerged for its potency against the HCV NS5B, with a calculated IC50 of 11-12 μM.

The Influence of Chlorine and Sulphonate Substituents on the Visible Absorption Maxima of Some Azo Dyes

A total of 110 arylazo dyes have been prepared, based on five benzenoid and heterocyclic coupling components, and containing combinations of chlorine and sulphonate (sulpho) substituents in the diazo components.Their visible absorption maxima have been analysed in order to determine the degree to which chloro and sulfo substituent influences are constant and transferable, both within a series, and between series.Additivity is found to pertain, if allowances are made for steric effects.A 2-sulpho group alone can induce nonplanarity, depending on the nature of the coupling component.The 2-sulpho-3-chloro combination is particularly responsible for hypsochromic shifts unexpected on the basis of strict additivity.Computer-aided molecular modelling studies have clarified the steric interactions present.Di-ortho-substitution also induces nonplanarity and hypsochromic effects.There is some evidence for non-equivalence of a substituent in the two distinct meta-orientations, although MO calculations do not reproduce this behaviour.

Method for the control of cattle grubs employing a phenylene bis[imino(thio]carbonyl)diphosphor(thio)-amidic acid ester

There is provided a method for controlling the larvae of heel flies which parasitize ruminants and other warm-blooded animals by administering to said animals an effective amount of an unsubstituted or substituted phenylene bis[imino(thio)carbonyl]diphosp