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Home > Encyclopedia > 1,3-Dichloro-2-nitrobenzene

1,3-Dichloro-2-nitrobenzene

1,3-Dichloro-2-nitrobenzene structure

1,3-Dichloro-2-nitrobenzene 

structure
  • CAS No:

    601-88-7

  • Formula:

    C6H3Cl2NO2

  • Chemical Name:

    1,3-Dichloro-2-nitrobenzene

  • Synonyms:

    Benzene,1,3-dichloro-2-nitro-;1,3-Dichloro-2-nitrobenzene;2,6-Dichloronitrobenzene;2,6-Dichloro-1-nitrobenzene

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

CRYSTALS.


CRYSTALS.

1,3-Dichloro-2-nitrobenzene Basic Attributes

192

192.00

210-009-3

0253

1578

DTXSID00208847

2904909090

Characteristics

45.8

3

CRYSTALS.

1.6 g/cm3

72.5 °C

130 °C @ Press: 8.3 Torr

118.9ºC

1.595

Relative vapour density (air = 1): 6.6

Safety Information

1578

T: Toxic;

Separated from bases and strong oxidants.

P273, P280, P302+P352, P312, P322, P363, P501

H312

Combustible.

|Warning|H312 (89.47%): Harmful in contact with skin [Warning Acute toxicity, dermal]|P273, P280, P302+P352, P312, P322, P363, and P501|Aggregated GHS information provided by 38 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Use powder, alcohol-resistant foam, water spray, carbon dioxide.

Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting.

Separated from bases and strong oxidants.

A nuisance-causing concentration of airborne particles can be reached quickly when dispersed.

NO open flames.

PREVENT DISPERSION OF DUST!

Use ventilation (not if powder).

Protective gloves.

Wear safety spectacles.

Drug Information

Fresh air, rest.


Rinse and then wash skin with water and soap.


Rinse with plenty of water (remove contact lenses if easily possible).

Cough.


Redness.

1,3-Dichloro-2-nitrobenzene Use and Manufacturing

1.32 g (4.0 mmol) of sodium tungstate dihydrate and 4.0 g (40 mmol) of concentrated sulfuric acid were added to a solution of 16.2 g (100 mmol) of 2, 6-dichloroaniline in 120 ml of methanol, and the mixture was heated to 40° C. 30 ml (291 mmol) of a 30percent hydrogen peroxide solution was added dropwise over 10 hours. 2.1.5. 1, 3-Dichloro-2-nitrobenzene [4] A solution of 2, 6-dichloroaniline (8.10 g, 50.0 mmol) in dichloromethane (200 mL) was cooledto 0 °C before a solution of 3-chloroperbenzoic acid (24.6 g, 100 mmol) in dichloromethane(250 mL) was added dropwise to the reaction mixture over a period of 1.5 h at 0 °C.Thereafter the solution was stirred for 2 h at room temperature before it was diluted withdichloromethane (250 mL). The reaction mixture was washed two times with an aqueoussodium thiosulfate solution (2 wt percent, 2 × 100 mL), with an aqueous sodium bicarbonatesolution (4 × 50 mL), and finally with deionized water (200 mL). The organic layer was driedwith magnesium sulfate and the solvent was removed in vacuo. The residue was suspendedin 40 mL n-hexane and irradiated by ultrasound for 5 min, filtered off, washed with n-hexane(2 × 20 mL) to give 1, 3-dichloro-2-nitrobenzene (6.63 g, 37.7 mmol, 75percent) as a beige solid

Computed Properties

Molecular Weight:192.00
XLogP3:3
Hydrogen Bond Acceptor Count:2
Exact Mass:190.9540837
Monoisotopic Mass:190.9540837
Topological Polar Surface Area:45.8
Heavy Atom Count:11
Complexity:149
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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