2-CHLORO-4,5-DIAMINOBENZOTRIFLUORIDE
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
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.
Safety Information
- Hazard Codes
- Xi
- Hazard Note
- Irritant
- HazardClass
- 6.1
- HS Code
- 2921599090
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
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