Ordering
Available Variants25 g
CHA.39580-25g
Price
€48.48
Available – Dispatch in 14 days
100 g
CHA.39580-100g
Price
€112.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.39580-25g | €48.48 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.39580-100g | €112.00 |
95%
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) | C4H2Br2S |
|---|---|
| CAS Number | 3141-27-3 |
| Molecular Weight | 241.93 |
| NACRES | NA.22 |
| PubChem Substance ID | 24846807 |
| UNSPSC Code | 12352100 |
| EC Number | 221-547-3 |
| MDL number | MFCD00005420 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 10 - Combustible liquids |
| wgk | WGK 3 |
| flash_point_f | 210.2 °F - closed cup |
| flash_point_c | 99 °C - closed cup |
| ppe | Eyeshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
2,5-Dibromothiophene, with the CAS registry number 3141-27-3, is a halogenated thiophene derivative that has garnered significant attention in the realm of organic chemistry. This compound is characterized by the presence of two bromine atoms at the 2 and 5 positions of the thiophene ring, which imparts unique chemical and physical properties. The dibromination of thiophene is typically achieved through electrophilic aromatic substitution reactions, and the resulting compound can serve as a versatile intermediate in the synthesis of various thiophene-based materials. 2,5-Dibromothiophene has been utilized in the preparation of conducting polymers, pharmaceuticals, and other specialty chemicals, highlighting its importance in modern synthetic chemistry. Its reactivity and potential applications continue to be explored by researchers, driving further innovation in the field of thiophene chemistry.
