Basic information Safety Supplier Related

3,4-DIAMINOBENZOTRIFLUORIDE

Basic information Safety Supplier Related

3,4-DIAMINOBENZOTRIFLUORIDE Basic information

Product Name:
3,4-DIAMINOBENZOTRIFLUORIDE
Synonyms:
  • Trifluoromethylbenzene, 3,4-diamine-
  • BUTTPARK 51\01-88
  • 4-(TRIFLUOROMETHYL)-1,2-PHENYLENEDIAMINE
  • 4-(TRIFLUOROMETHYL)-O-PHENYLENEDIAMINE
  • 4-(TRIFLUOROMETHYL)BENZENE-1,2-DIAMINE
  • 3,4-DIAMINOBENZOTRIFLUORIDE
  • 3,4-DIAMINOTRIFLUOROMETHYLBENZENE
  • 4-(Trifluoromethyl)-1,2-benzenediamine
CAS:
368-71-8
MF:
C7H7F3N2
MW:
176.14
Product Categories:
  • Aromatic Halides (substituted)
  • Amines and Anilines
  • Benzotrifluoride Series
Mol File:
368-71-8.mol
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3,4-DIAMINOBENZOTRIFLUORIDE Chemical Properties

Melting point:
56-58 °C
Boiling point:
253℃
Density 
1.381
Flash point:
111℃
storage temp. 
2-8°C(protect from light)
pka
2.94±0.10(Predicted)
form 
powder
color 
Light brown to brown
Water Solubility 
Miscible with water.
BRN 
909258
CAS DataBase Reference
368-71-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-20/21/22-22
Safety Statements 
36/37/39-26
RIDADR 
2811
Hazard Note 
Harmful/Irritant
HazardClass 
IRRITANT-HARMFUL
HazardClass 
6.1
PackingGroup 
HS Code 
29215900

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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3,4-DIAMINOBENZOTRIFLUORIDE Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Uses

3,4-Diaminobenzotrifluoride is commonly used as pharmaceutical intermediate.

Synthesis

7732-18-5

400-98-6

368-71-8

The reaction was carried out in anhydrous ethanol (50 mL) at reflux for 45 minutes with 4-amino-3-nitrobenzotrifluoride (5.000 g, 24.26 mmol, Aldrich, direct use) and SnCl2-2H2O (20.00 g, 88.64 mmol, Aldrich, direct use). Upon completion of the reaction, the mixture was poured into ice (85 g) and alkalized with 10% aqueous NaHCO3 (250 mL). Subsequently, the resulting suspension was extracted with ethyl acetate (400 mL). The ethyl acetate extracts were combined, dried with Na2SO4, and the solvent was evaporated under reduced pressure to give 4.14 g (87% yield) of pure 4-trifluoromethyl-1,2-phenylenediamine as a red powder.

References

[1] Patent: US5514680, 1996, A

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