Basic information Safety Supplier Related

3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID

Basic information Safety Supplier Related

3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID Basic information

Product Name:
3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID
Synonyms:
  • RARECHEM AL BO 1012
  • 3-TRIFLUOROMETHYL-5-NITROBENZOIC ACID
  • 3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID
  • 3-CARBOXY-5-NITROBENZOTRIFLUORIDE
  • A,A,A-TRIFLUORO-5-NITRO-M-TOLUIC ACID
  • LABOTEST-BB LT00454389
  • BUTTPARK 25\01-30
  • 5-(Trifluoromethyl)-3-nitrobenzoic acid
CAS:
328-80-3
MF:
C8H4F3NO4
MW:
235.12
EINECS:
630-023-7
Product Categories:
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
Mol File:
328-80-3.mol
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3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID Chemical Properties

Melting point:
128 °C
Boiling point:
309.9±42.0 °C(Predicted)
Density 
1.596±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
3.05±0.10(Predicted)
color 
White to Light yellow to Light orange
BRN 
2284651
CAS DataBase Reference
328-80-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-60-37
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

  • Language:English Provider:ALFA
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3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID Usage And Synthesis

Synthesis

454-92-2

328-80-3

The general procedure for synthesizing 3-nitro-5-(trifluoromethyl)benzoic acid from 3-trifluoromethylbenzoic acid is as follows: 1. 90% fuming nitric acid (210 mL) was slowly added to a solution of concentrated sulfuric acid (880 mL) of 3-trifluoromethylbenzoic acid (203.4 g) at 0 °C, and the addition process continued for 1 hour. 2. the reaction mixture was stirred at 35°C for 3 hours. 3. The reaction solution was slowly poured into ice (about 1 kg) to precipitate the product. 4. The precipitate was collected by filtration and washed with water (500 mL). 5. The precipitate was dissolved in ethyl acetate (500 mL) and the organic phase was washed with water. 6. After drying the organic phase, the solvent was evaporated under reduced pressure to give 3-nitro-5-(trifluoromethyl)benzoic acid (232.5 g, 92% yield) as a white powder. 1H-NMR (300MHz, CDCl3): δ 8.69 (1H, s), 8.74 (1H, s), 9.1 (1H, s).

References

[1] Patent: US2008/275085, 2008, A1. Location in patent: Page/Page column 45
[2] Journal of the American Chemical Society, 2017, vol. 139, # 43, p. 15308 - 15311
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 6, p. 2362 - 2380
[4] Angewandte Chemie - International Edition, 2017, vol. 56, # 8, p. 2059 - 2063
[5] Angew. Chem., 2017, vol. 129, # 8, p. 2091 - 2095,5

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