Ordering
Available Variants5 g
CHA.97249-5g
Price
€21.36
Available – Dispatch in 14 days
25 g
CHA.97249-25g
Price
€64.24
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.97249-5g | €21.36 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.97249-25g | €64.24 |
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 | 402-23-3 |
| Molecular Weight | 239.03 |
| NACRES | NA.22 |
| PubChem Substance ID | 24857473 |
| UNSPSC Code | 12352100 |
| EC Number | 206-938-9 |
| MDL number | MFCD00000395 |
| Assay | 98% |
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 | 190.4 °F - closed cup |
| flash_point_c | 88 °C - closed cup |
| ppe | Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
3-(Trifluoromethyl)benzyl bromide, with the CAS registry number 402-23-3, is a chemical compound that has been utilized in various organic synthesis reactions. This compound is a trifluoromethyl-substituted benzyl bromide, which exhibits unique properties due to the presence of the trifluoromethyl group. The trifluoromethyl group is known for its high electronegativity and ability to participate in various chemical reactions, making 3-(Trifluoromethyl)benzyl bromide a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactivity and versatility have led to its application in numerous fields, including medicinal chemistry and materials science, where the introduction of fluorine-containing functional groups is often desirable. As a result, 3-(Trifluoromethyl)benzyl bromide has become an important building block in modern organic synthesis.
