Basic information Safety Supplier Related

2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDE

Basic information Safety Supplier Related

2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDE Basic information

Product Name:
2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDE
Synonyms:
  • 2-AMino-4-chloro-5-(trifluoroMethyl)aniline
  • 2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDE
  • 4-CHLORO-5-TRIFLUOROMETHYL-BENZENE-1,2-DIAMINE
  • 2-Amino-4-chloro-5-(trifluoromethyl)phenylamine
  • 3,4-Diamino-6-chlorobenzotrifluoride
  • 5-Chloro-4-(trifluoromethyl)benzene-1,2-diamine
  • 4-Chloro-5-trifluoroMethyl-o-phenylenediaMine, 95%
  • 4-Chloro-5-(trifluoromethyl)benzene-1,2-diamine 97%
CAS:
157590-59-5
MF:
C7H6ClF3N2
MW:
210.58
Mol File:
Mol File
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2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDE Chemical Properties

Melting point:
61-63°
Boiling point:
305.1±42.0 °C(Predicted)
Density 
1.510
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
2.30±0.10(Predicted)
form 
Solid
color 
White to brown
Water Solubility 
Slightly soluble in water.
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HazardClass 
6.1
HS Code 
2921599090
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2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDE Usage And Synthesis

Uses

4-Chloro-5-trifluoromethyl-o-phenylenediamine has application in dietary supplements, pharmaceutical or cosmeticeuticals.

Synthesis

35375-74-7

157590-59-5

General procedure for the synthesis of 2-chloro-4,5-diaminotrifluoromethylbenzene from 5-chloro-2-nitro-4-(trifluoromethyl)aniline: 5-chloro-2-nitro-4-(trifluoromethyl)aniline (2 g, 8.31 mmol) was dissolved in a solvent mixture of EtOH:H2O (5:1, 10 mL) at room temperature. Subsequently, SnCl2 (4.73 g, 24.9 mmol) was added to the solution. The reaction mixture was stirred at 80°C for 3 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was filtered through a bed of diatomaceous earth and the filtrate was concentrated under reduced pressure to afford 4-chloro-5-(trifluoromethyl)benzene-1,2-diamine as a yellow semi-solid product. Yield: 1.7 g, 97% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 6.95 (s,1H), 6.88 (s,1H), 4.68-5.08 (bs,4H). Mass spectrometry (ESI-) analysis showed m/z 209.15 [M-H]-.

References

[1] Patent: WO2018/37223, 2018, A1. Location in patent: Page/Page column 118; 119
[2] Journal of Medicinal Chemistry, 1995, vol. 38, # 22, p. 4367 - 4379
[3] Patent: WO2004/35549, 2004, A1. Location in patent: Page 105
[4] Patent: WO2008/56150, 2008, A1. Location in patent: Page/Page column 182

2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDESupplier

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