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Available Variants5 g
CHA.26900-5g
Price
€67.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.26900-5g | €67.80 |
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.
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Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C4H2I2S |
|---|---|
| CAS Number | 625-88-7 |
| Molecular Weight | 335.93 |
| NACRES | NA.22 |
| PubChem Substance ID | 24859977 |
| UNSPSC Code | 12352100 |
| EC Number | 210-915-9 |
| MDL number | MFCD00014525 |
| Assay | 98% |
| Form | solid |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | 204.8 °F - closed cup |
| flash_point_c | 96.00 °C - closed cup |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
2,5-Diiodothiophene, with the CAS number 625-88-7, 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 iodine atoms attached to the 2 and 5 positions of the thiophene ring, resulting in a molecule with unique electronic and optical properties. The synthesis of 2,5-diiodothiophene typically involves the iodination of thiophene, which can be achieved through various methods, including electrophilic aromatic substitution reactions. This compound serves as a valuable intermediate in the preparation of a wide range of materials, including conducting polymers, organic semiconductors, and pharmaceuticals, owing to its ability to undergo cross-coupling reactions and other functionalization processes. Its reactivity and versatility make 2,5-diiodothiophene a crucial building block in modern organic synthesis.
