| 3-(Trifluoromethyl)benzaldehyde Basic information |
| Uses |
| Product Name: | 3-(Trifluoromethyl)benzaldehyde |
| Synonyms: | m-Trifluoromethoxy benzaldehyde;3-Formylbenzotrifluoride, alpha,alpha,alpha-Trifluoro-3-tolualdehyde;Alpha-Trifluoro-M-tolualdehyde;3-(TrifluoroMethyl)benzaldehyde, 97% 25GR;3-(TrifluoroMethyl)benzaldehyde, 97% 5GR;3-Formylbenzotrifluoride, alpha,alpha,alpha-Trifluoro-m-tolualdehyde;3-(three fluoroMethyl)benzeneforMaldehyde;Between the three groups in benzene forMaldehyde |
| CAS: | 454-89-7 |
| MF: | C8H5F3O |
| MW: | 174.12 |
| EINECS: | 207-228-1 |
| Product Categories: | Benzotrifluoride Series;Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;3-(Trifluoromethyl)benzaldehyde;bc0001 |
| Mol File: | 454-89-7.mol |
| 3-(Trifluoromethyl)benzaldehyde Chemical Properties |
| Boiling point | 83-86 °C30 mm Hg(lit.) |
| density | 1.301 g/mL at 25 °C(lit.) |
| refractive index | n |
| Fp | 155 °F |
| storage temp. | Keep in dark place,Sealed in dry,Room Temperature |
| form | Liquid |
| color | Clear colorless to very slightly orange |
| Specific Gravity | 1.301 |
| Sensitive | Air Sensitive |
| BRN | 2327537 |
| InChIKey | NMTUHPSKJJYGML-UHFFFAOYSA-N |
| CAS DataBase Reference | 454-89-7(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzaldehyde, 3-(trifluoromethyl)-(454-89-7) |
| EPA Substance Registry System | Benzaldehyde, 3-(trifluoromethyl)- (454-89-7) |
| Safety Information |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36 |
| RIDADR | UN3082 - class 9 - PG 3 - DOT NA1993 - Environmentally hazardous substances, liquid, n.o.s. HI: all (not BR) |
| WGK Germany | 3 |
| F | 10-23 |
| TSCA | T |
| HazardClass | IRRITANT |
| HS Code | 29130000 |
| MSDS Information |
| Provider | Language |
|---|---|
| alpha,alpha,alpha-Trifluoro-3-tolualdehyde | English |
| ACROS | English |
| SigmaAldrich | English |
| ALFA | English |
| 3-(Trifluoromethyl)benzaldehyde Usage And Synthesis |
| Uses | 3-(Trifluoromethyl)benzaldehyde is used as a reagent in the synthesis of 2,3-di- and 2,2,3-trisubstituted-3-methoxycarbonyl-γ-butyrolactones as potent antitumor agents. Also used as a reagent in the synthesis of novel chalcone derivatives as hypoxia-inducible factor (HIF)-1 inhibitors. |
| Chemical Properties | CLEAR COLOURLESS TO VERY SLIGHTLY ORANGE LIQUID |
| Synthesis Reference(s) | Journal of the American Chemical Society, 68, p. 426, 1946 DOI: 10.1021/ja01207a024 |
| General Description | Aldol reaction of 3-(trifluoromethyl)benzaldehyde with hydroxyacetone in the aldolase antibody 38C2-ionic liquid system has been investigated. |
| 3-(Trifluoromethyl)benzaldehyde Preparation Products And Raw materials |
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