Name | 4-(Trifluoromethyl)benzyl chloride |
Synonyms | TIMTEC-BB SBB006696 4-Trifluoromethylbenzyl chloride à'-chloro-à,à,à-trifluoro-p-xylene 4-(Trifluoromethyl)benzyl chloride P-(TRIFLUOROMETHYL)BENZYL CHLORIDE 4-(TRIFLUOROMETHYL)BENZYL CHLORIDE α'-chloro-α,α,α-trifluoro-p-xylene 1-(chloromethyl)-4-(trifluoromethyl)benzene 1-(CHLOROMETHYL)-4-(TRIFLUOROMETHYL)BENZENE ALPHA'-CHLORO-ALPHA,ALPHA,ALPHA-TRIFLUORO-P-XYLENE |
CAS | 939-99-1 |
InChI | InChI=1/C8H6ClF3/c9-5-6-1-3-7(4-2-6)8(10,11)12/h1-4H,5H2 |
Molecular Formula | C8H6ClF3 |
Molar Mass | 194.58 |
Density | 1.315g/mLat 25°C(lit.) |
Melting Point | 19 °C |
Boling Point | 68°C12mm Hg(lit.) |
Flash Point | 165°F |
Vapor Presure | 0.793mmHg at 25°C |
Appearance | clear liquid |
Color | Colorless to Almost colorless |
BRN | 511085 |
Storage Condition | Refrigerator |
Sensitive | Lachrymatory |
Refractive Index | n20/D 1.464(lit.) |
Physical and Chemical Properties | This product is colorless liquid, B. P. 68 ℃/1.6kPa,n20D 1.4622, insoluble in water, soluble in benzene, toluene and other organic solvents. |
Hazard Symbols | C - Corrosive |
Risk Codes | R34 - Causes burns R36/37 - Irritating to eyes and respiratory system. |
Safety Description | S23 - Do not breathe vapour. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S27 - Take off immediately all contaminated clothing. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 3265 8/PG 2 |
WGK Germany | 3 |
HS Code | 29039990 |
Hazard Note | Corrosive/Lachrymatory |
Hazard Class | 8 |
Packing Group | III |
Use | 4-(chloromethyl) trifluoromethyl benzene is an intermediate of the rodenticide fluorosperm. |
Production method | The preparation method is to use p-trifluoromethyl benzaldehyde as raw material, dissolve in methanol, and add sodium borohydride for reduction to obtain p-trifluoromethyl benzyl alcohol, and then react with thionyl chloride to obtain the product. |