ChemicalBook--->CAS DataBase List--->328-68-7

328-68-7

328-68-7 Structure

328-68-7 Structure
IdentificationMore
[Name]

3-Amino-5-(trifluoromethyl)benzoic acid
[CAS]

328-68-7
[Synonyms]

3-AMINO-5-(TRIFLUOROMETHYL)BENZOIC ACID
BUTTPARK 25\01-23
3-Amino-5-(trifluoromethyl)benzoic acid 97%
3-AMINO-5-(TRIFLUOROEMTHYL)BENZOIC ACID
3-Amino-5-(trifluoromethyl)benzoicacid97%
[Molecular Formula]

C8H6F3NO2
[MDL Number]

MFCD00236641
[Molecular Weight]

205.13
[MOL File]

328-68-7.mol
Chemical PropertiesBack Directory
[Melting point ]

141-146 °C(lit.)
[Boiling point ]

331.9±42.0 °C(Predicted)
[density ]

1.489±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

powder to crystal
[pka]

3.93±0.10(Predicted)
[color ]

Light yellow to Yellow to Orange
[Major Application]

peptide synthesis
[InChI]

1S/C8H6F3NO2/c9-8(10,11)5-1-4(7(13)14)2-6(12)3-5/h1-3H,12H2,(H,13,14)
[InChIKey]

WBTHOSZMTIPJLR-UHFFFAOYSA-N
[SMILES]

Nc1cc(cc(c1)C(F)(F)F)C(O)=O
[CAS DataBase Reference]

328-68-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[RIDADR ]

UN 2811 6.1/PG 3
[WGK Germany ]

3
[RTECS ]

DD6205700
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

peptide synthesis
[reaction suitability]

reaction type: solution phase peptide synthesis
[Synthesis]

3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID

328-80-3

3-Amino-5-(trifluoromethyl)benzoic acid

328-68-7

The suspension formed by 3-nitro-5-(trifluoromethyl)benzoic acid (103 g x 2 batches) obtained in step 1 and 10% palladium-carbon catalyst (5.15 g x 2 batches) in ethanol (1500 mL x 2 batches) was placed under the atmosphere of hydrogen at 1 atmospheric pressure, and the reaction was stirred for 7 hours at room temperature. After completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to afford the target product 3-amino-5-(trifluoromethyl)benzoic acid (180 g, 100% yield) as a light yellow powder. The product was characterized by 1H-NMR (300 MHz, CDCl3): δ 4.00-6.00 (2H, broad peak), 7.10 (1H, single peak), 7.53 (1H, single peak), 7.72 (1H, single peak).

[References]

[1] Patent: US2008/275085, 2008, A1. Location in patent: Page/Page column 45
[2] Chemistry - A European Journal, 2017, vol. 23, # 52, p. 12758 - 12762
[3] Patent: US2007/213371, 2007, A1. Location in patent: Page/Page column 70
[4] Journal of the American Chemical Society, 2017, vol. 139, # 43, p. 15308 - 15311
[5] Patent: WO2004/29038, 2004, A1. Location in patent: Page 44
Spectrum DetailBack Directory
[Spectrum Detail]

3-Amino-5-(trifluoromethyl)benzoic acid(328-68-7)1HNMR
3-Amino-5-(trifluoromethyl)benzoic acid(328-68-7)FT-IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

328-68-7(sigmaaldrich)
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