| 3'-(Trifluoromethyl)acetophenone Basic information |
| Product Name: | 3'-(Trifluoromethyl)acetophenone |
| Synonyms: | 3'-(Trifluoromethyl)acetophenone,99%;3-Trifludromethylacetophen;1-[3-(Trifluoromethyl)phenyl]ethan-1-one, 3-Acetylbenzotrifluoride;3'-(TrifluoroMethyl)acetophenone, 97+%;1-[3-(Trifluoromethyl)phenyl]-1-ethanone;3-ACETYLBENZOTRIFLUORIDE;3-ACETYLBENZOFLUORIDE;3'-(TRIFLUOROMETHYL)ACETOPHENONE |
| CAS: | 349-76-8 |
| MF: | C9H7F3O |
| MW: | 188.15 |
| EINECS: | 206-490-4 |
| Product Categories: | Building Blocks;C9;Carbonyl Compounds;Chemical Synthesis;Ketones;Organic Building Blocks;Multisubstituted Benzene;Aromatic Acetophenones & Derivatives (substituted);Organics;Benzene series;bc0001 |
| Mol File: | 349-76-8.mol |
| 3'-(Trifluoromethyl)acetophenone Chemical Properties |
| Boiling point | 198-200 °C(lit.) |
| density | 1.235 g/mL at 25 °C(lit.) |
| vapor pressure | 35Pa at 25℃ |
| refractive index | n |
| Fp | 183 °F |
| storage temp. | Sealed in dry,Room Temperature |
| form | clear liquid |
| Specific Gravity | 1.235 |
| color | Colorless to Red to Green |
| Water Solubility | 620mg/L at 25℃ |
| BRN | 640151 |
| InChIKey | ABXGMGUHGLQMAW-UHFFFAOYSA-N |
| LogP | 2.55 at 25℃ |
| CAS DataBase Reference | 349-76-8(CAS DataBase Reference) |
| NIST Chemistry Reference | 3-CF3-C6H4-COCH3(349-76-8) |
| EPA Substance Registry System | Ethanone, 1-[3-(trifluoromethyl)phenyl]- (349-76-8) |
| Safety Information |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36 |
| WGK Germany | 1 |
| TSCA | Yes |
| HazardClass | IRRITANT |
| HS Code | 29147090 |
| MSDS Information |
| Provider | Language |
|---|---|
| 3-Acetylbenzotrifluoride | English |
| ACROS | English |
| SigmaAldrich | English |
| ALFA | English |
| 3'-(Trifluoromethyl)acetophenone Usage And Synthesis |
| Chemical Properties | CLEAR COLOURLESS TO VERY SLIGHTLY YELLOW LIQUID |
| Uses | 3''-?(Trifluoromethyl)?acetophenone is a reagent used in the stabilization of endosomal-toll-like receptor TRL8 creating a sort of inhibitory activity. |
| General Description | Asymmetric catalytic addition of ethyl groups to 3′-(trifluoromethyl)acetophenone catalyzed by ligands derived from trans-1,2-diaminocyclohexane and camphor sulfonyl chloride has been reported. Phenylation of 3′-(trifluoromethyl)acetophenone in the presence of dihydroxy bis(sulfonamide) ligand (enantioselective catalyst), titanium tetraisopropoxide and diphenylzinc has been investigated. |
| 3'-(Trifluoromethyl)acetophenone Preparation Products And Raw materials |
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