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Available Variants5 g
CHA.52002-5g
Price
€39.12
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.52002-5g | €39.12 |
97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | FC6H3(CF3)COCl |
|---|---|
| CAS Number | 189807-21-4 |
| Molecular Weight | 226.56 |
| NACRES | NA.22 |
| PubChem Substance ID | 24869064 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00061158 |
| Assay | 97% |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H314 |
| pcodes | P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405 |
| Hazard Classifications | Skin Corr. 1B |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| flash_point_f | 185.0 °F - closed cup |
| flash_point_c | 85 °C - closed cup |
| ppe | Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
4-Fluoro-2-(trifluoromethyl)benzoyl chloride, with the CAS registry number 189807-21-4, is a chemical compound that belongs to the class of acyl chlorides. This compound is characterized by the presence of a fluorine atom and a trifluoromethyl group attached to a benzene ring, which is further functionalized with a carbonyl chloride moiety. The unique combination of fluorine and trifluoromethyl substituents imparts distinct chemical and physical properties to this compound, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The reactivity of the acyl chloride functional group allows it to participate in a range of chemical reactions, including nucleophilic substitution and addition reactions, making 4-fluoro-2-(trifluoromethyl)benzoyl chloride a versatile building block in organic synthesis. Its applications are diverse and continue to expand.
