Name | 3,5-Bis(trifluoromethyl)benzoyl chloride |
Synonyms | FXFFR CVG EXFFF Benzoyl Chloride, 3 3,5-BIS(TRIFLUOROMETHYL)BENZOYCHLORIDE 3,5-di(Trifluoromethyl)benzoyl chloride 3,5-Bis(trifluoromethyl)benzoyl chloride Benzoyl chloride, 3,5-bis(trifluoromethyl)- 3,5-Bis(trifluoromethyl)benzoic acid chloride [3,5-bis(trifluoroMethyl)phenyl]carbonylchloranuide trichloro(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)silane |
CAS | 785-56-8 |
EINECS | 212-322-0 |
InChI | InChI=1/C10H4Cl3F17Si/c11-31(12,13)2-1-3(14,15)4(16,17)5(18,19)6(20,21)7(22,23)8(24,25)9(26,27)10(28,29)30/h1-2H2 |
Molecular Formula | C9H3ClF6O |
Molar Mass | 276.56 |
Density | 1.526g/mLat 25°C(lit.) |
Melting Point | 5-10C |
Boling Point | 65-67 °C (12 mmHg) |
Flash Point | 162°F |
Vapor Presure | 0.0865mmHg at 25°C |
Appearance | Liquid |
Specific Gravity | 1.526 (20/4℃) |
Color | Clear colorless to very slightly yellow |
BRN | 2593440 |
Storage Condition | Room Temprature |
Sensitive | Moisture Sensitive |
Refractive Index | n20/D 1.435(lit.) |
MDL | MFCD00000387 |
Hazard Symbols | C - Corrosive |
Risk Codes | R34 - Causes burns R37 - Irritating to the respiratory system R36 - Irritating to the eyes |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 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.) S27 - Take off immediately all contaminated clothing. |
UN IDs | UN 3265 8/PG 2 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10-19-21 |
HS Code | 29163990 |
Hazard Note | Corrosive |
Hazard Class | 8 |
Packing Group | II |
Application | is an important organic synthesis intermediate with wide application and good prospect in medicine, pesticide and various functional materials. For the synthesis of 3, 5-bis (trifluoromethyl) benzoyl structure characterized by neurokinin antagonist drugs, as well as a class of chlorine-containing herbicides. It can also be used to synthesize an efficient catalyst for the dehydrogenation of germanium and alkanes, and the sodium salt of the acid is also an excellent antioxidant. |