![2,3-Dibromobenzo[b]thiophene molecular structure](/images/molecules/2-3-dibromobenzo-b-thiophene-6287-82-7.png)
Ordering
Available Variants5 g
CHA.70784-5g
Price
€75.36
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.70784-5g | €75.36 |
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
| Empirical Formula (Hill Notation) | C8H4Br2S |
|---|---|
| CAS Number | 6287-82-7 |
| Molecular Weight | 291.99 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883530 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD06798119 |
| Assay | 97% |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS06
 GHS06
|
|---|---|
| signalword | Danger |
| hcodes | H301,H319,H413 |
| pcodes | P264 - P273 - P280 - P301 + P310 - P305 + P351 + P338 - P337 + P313 |
| Hazard Classifications | Acute Tox. 3 Oral - Aquatic Chronic 4 - Eye Irrit. 2 |
| Storage Class | 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
2,3-Dibromobenzo[b]thiophene, with a CAS number of 6287-82-7, is a halogenated heterocyclic compound that has garnered significant attention in the realm of organic chemistry. This compound is characterized by the presence of two bromine atoms attached to the 2 and 3 positions of the benzo[b]thiophene ring system. The unique structural features of 2,3-dibromobenzo[b]thiophene render it a valuable intermediate in the synthesis of various complex molecules, including pharmaceuticals and materials science applications. Its reactivity profile, which is influenced by the bromine substituents and the inherent properties of the thiophene ring, makes it an attractive substrate for further functionalization and transformation into a wide range of derivatives. As such, 2,3-dibromobenzo[b]thiophene is a versatile building block in modern organic synthesis.
