| Identification | More | [Name]
4-Fluoro-2-(trifluoromethyl)benzaldehyde | [CAS]
90176-80-0 | [Synonyms]
2-TRIFLUOROMETHYL-4-FLUOROBENZALDEHYDE
4-FLUORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE
2-Trifluoromethoxy-4-Fluorobenzaldehyde 4-Fluoro-2-(Trifluoromethyl) Benzaldehyde
2-Trifluoromethoxy-4-Fluorobenzaldehyde
4-Fluoro-2-(trilfuoromethyl)benzaldehyde
alpha,alpha,alpha,4-Tetrafluoro-o-tolualdehyde
4-Fluoro-2-(Trifluoromethyl)be
à,à,à,4-tetrafluoro-o-tolualdehyde
4-Fluoro-2-(trifluoromethyl)benzaldehyde 97%
4-Fluoro-2-(trifluoromethyl)benzaldehyde97%
Benzaldehyde, 4-fluoro-2-(trifluoromethyl)- | [Molecular Formula]
C8H4F4O | [MDL Number]
MFCD00061313 | [Molecular Weight]
192.11 | [MOL File]
90176-80-0.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless liquid | [Boiling point ]
114 °C (lit.) | [density ]
1.408 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.452(lit.)
| [Fp ]
134 °F
| [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [Sensitive ]
Air Sensitive | [BRN ]
5932091 | [CAS DataBase Reference]
90176-80-0(CAS DataBase Reference) |
| Safety Data | Back 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 .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 1989 3/PG 3
| [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29130000 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless liquid | [Uses]
Starting material for Fevipiprant. 4-Fluoro-2-(trifluoromethyl)benzaldehyde is also a reagent in the preparation of numerous inhibitors against proteins such as CRTH2, DP2 Receptor and Hepatitis B Virus (HBV) Capsid. | [General Description]
4-Fluoro-2-(trifluoromethyl)benzaldehyde is an organic fluorinated building block. It participates in the synthesis of diphenylthioethers. It also participates in the preparation of 1-cyano derivative of nilutamide. |
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