Ordering
Available Variants1 g
CHA.63944-1g
Price
€29.28
Available – Dispatch in 14 days
5 g
CHA.63944-5g
Price
€63.68
Available – Dispatch in 14 days
25 g
CHA.63944-25g
Price
€228.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.63944-1g | €29.28 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.63944-5g | €63.68 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.63944-25g | €228.80 |
98%
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 | CF3C6H4CH2Br |
|---|---|
| CAS Number | 402-49-3 |
| Molecular Weight | 239.03 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 24857474 |
| EC Number | 206-947-8 |
| Beilstein/REAXYS Number | 638980 |
| MDL number | MFCD00000403 |
| Assay | 98% |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H314 |
| pcodes | P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 |
| Hazard Classifications | Skin Corr. 1B |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| ppe | Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
4-(Trifluoromethyl)benzyl bromide, with the CAS registry number 402-49-3, is a chemical compound that has garnered significant attention in various fields of research. This organic compound is characterized by the presence of a trifluoromethyl group attached to a benzene ring, which is further functionalized with a benzyl bromide moiety. The unique combination of functional groups in this molecule imparts distinct chemical and physical properties, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. The trifluoromethyl group, in particular, is known to influence the molecular properties, such as lipophilicity and stability, which can be advantageous in the design of biologically active molecules. As a result, 4-(trifluoromethyl)benzyl bromide has become a sought-after building block in modern organic synthesis.
