Name | alpha,alpha,alpha-Trifluoro-p-tolualdehyde |
Synonyms | PTF-BAD 4-Trifluoromethylbenzaldehyde p-Trifluoromethylbenzaldehyde P-TRIFLUOROMETHYLBENZALDEHYDE α,α,α-Trifluoro-p-tolualdehyde 4-(trifluoromethy)benzaldehyde A,A,A-TRIFLUORO-P-TOLUALDEHYDE 4-(Trifluoromethyl)benzaldehyde P-(TRIFLUOROMETHYL)-BENZALDHYDE p-(Trifluoromethyl)benzaldehyde 4'-TRIFLUOROMETHYL BENZALDEHYDE 4-(TRIFLUOROMETHYL)BENZALDEHYDE p-(Trifluoromethyl) benzaldehyde 4-(Trifluoromethyl) benzaldehyde 4-(Trifluoromethyl)-benzaldehyde alpha,alpha,alpha-Trifluoro-p-tolualdehyde p-(Trifluoromethyl)benzaldehyde 4-(Trifluoromethyl)benzaldehyde |
CAS | 455-19-6 |
EINECS | 207-240-7 |
InChI | InChI=1/C8H5F3O/c9-8(10,11)7-3-1-6(5-12)2-4-7/h1-5H |
InChIKey | BEOBZEOPTQQELP-UHFFFAOYSA-N |
Molecular Formula | C8H5F3O |
Molar Mass | 174.12 |
Density | 1.275g/mLat 25°C(lit.) |
Melting Point | 1-2°C |
Boling Point | 66-67°C13mm Hg(lit.) |
Flash Point | 150°F |
Water Solubility | Soluble in water. 1.5 g/L at 20°C |
Solubility | 1.5g/l |
Vapor Presure | 1.09mmHg at 25°C |
Appearance | Transparent liquid |
Specific Gravity | 1.275 |
Color | Clear colorless to yellow |
BRN | 1101680 |
Storage Condition | Inert atmosphere,2-8°C |
Sensitive | Air Sensitive |
Refractive Index | n20/D 1.463(lit.) |
MDL | MFCD00006952 |
Physical and Chemical Properties | Density 1.275 boiling point 66-67 ° C (13 mmHg) flash point 65°C |
Use | Used in exercise studies in the Wittig reaction and in the asymmetric synthesis of alcohol. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10-23 |
TSCA | T |
HS Code | 29130000 |
Hazard Note | Irritant |
Hazard Class | IRRITANT, AIR SENSIT |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Synthesis method | Using p-trifluoromethylaniline as raw material, p-trifluoromethylbenzaldehyde is prepared by diazotization, oxime, and hydrolysis. The yield is 35.9%. The mixed solution of halogenated hydrocarbon additive and p-trifluoromethylchlorobenzene is slowly added to the tetrahydrofuran solution impregnated with magnesium chips to synthesize the Grignard reagent of p-trifluoromethylchlorobenzene; N,N-dimethylformamide is added to the Grignard reagent of p-trifluoromethyl chlorobenzene to react to obtain this product. |
Use | Kinetic research reagents for Wittig reactions and asymmetric synthesis reactions of alcohols |