Basic information Safety Supplier Related

5-CHLORO-4-METHYL-2-NITROANILINE

Basic information Safety Supplier Related

5-CHLORO-4-METHYL-2-NITROANILINE Basic information

Product Name:
5-CHLORO-4-METHYL-2-NITROANILINE
Synonyms:
  • TIMTEC-BB SBB003703
  • 5-CHLORO-2-NITRO-P-TOLUIDINE
  • 5-CHLORO-4-METHYL-2-NITROANILINE
  • 5-Chloro-4-methyl-2-nitroaniline, 95+%
  • [(pentylamino)-phosphonomethyl]phosphonic acid
  • 5-Chloro-4-methyl-2-nitroaniline,96%
  • 4-Amino-2-chloro-5-nitrotoluene
  • 5-Chloro-4-methyl-1-amino-2-nitrobenzene
CAS:
7149-80-6
MF:
C7H7ClN2O2
MW:
186.6
Product Categories:
  • Amines and Anilines
Mol File:
7149-80-6.mol
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5-CHLORO-4-METHYL-2-NITROANILINE Chemical Properties

Melting point:
159-163 °C
Boiling point:
339.3±37.0 °C(Predicted)
Density 
1.415±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
Crystalline Powder
pka
-0.79±0.25(Predicted)
color 
Orange-brown
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
HS Code 
29214200

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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5-CHLORO-4-METHYL-2-NITROANILINE Usage And Synthesis

Chemical Properties

orange-brown crystalline powder

Synthesis

7149-78-2

7149-80-6

(b) Preparation of the intermediate compound 5-chloro-4-methyl-2-nitroaniline: Sodium ethoxide (8.27 g, 45.9 mmol) was dissolved in ethanol (10 mL) to prepare a sodium ethoxide solution. The solution was slowly added to a solution of ethanol (10 mL) containing N-(2-nitro-4-methyl-5-chlorophenyl)acetamide (7.0 g, 30.6 mmol) with stirring at room temperature. After 1 hour of reaction, the reaction mixture was poured into water (100 mL) and precipitate was precipitated. The precipitate was collected by filtration and washed with a mixture of isopropanol and n-hexane (1:3, 10 mL) followed by n-hexane (10 mL) to give 5.71 g (85% yield) of 5-chloro-4-methyl-2-nitroaniline. Mass spectrometry (MS) showed a m/z of 187.0 (M + 1).

References

[1] Patent: WO2010/19208, 2010, A1. Location in patent: Page/Page column 167-168
[2] Journal of Medicinal Chemistry, 1992, vol. 35, # 23, p. 4455 - 4463
[3] Journal of Heterocyclic Chemistry, 1981, vol. 18, p. 1635 - 1636
[4] Patent: WO2011/23812, 2011, A1. Location in patent: Page/Page column 164

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