Ordering
Available Variants5 g
CHA.84791-5g
Price
€165.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.84791-5g | €165.60 |
96%
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
| Empirical Formula (Hill Notation) | C5H4Br2S |
|---|---|
| CAS Number | 40032-76-6 |
| Molecular Weight | 255.96 |
| NACRES | NA.23 |
| PubChem Substance ID | 329761461 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD02180908 |
| Assay | 96% |
| Form | liquid |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
  GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H302,H314 |
| pcodes | P260 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Oral - Skin Corr. 1B |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
2-Bromo-3-(bromomethyl)thiophene, with the CAS number 40032-76-6, is a halogenated thiophene derivative that has garnered significant attention in the realm of organic chemistry. This compound exhibits a molecular structure comprising a thiophene ring with bromine substituents at the 2 and 3 positions, as well as a bromomethyl group attached to the 3-position. The presence of these bromine atoms renders the molecule highly reactive, making it a valuable intermediate in various synthetic transformations. As such, 2-Bromo-3-(bromomethyl)thiophene has been employed in the synthesis of complex molecules, including pharmaceuticals and materials science applications, where its unique reactivity profile can be leveraged to form novel compounds with distinct properties. Its reactivity and versatility have made it a sought-after compound in research and development endeavors.
