Ordering
Available Variants1 g
CHA.47344-1g
Price
€92.80
Available – Dispatch in 14 days
5 g
CHA.47344-5g
Price
€283.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.47344-1g | €92.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.47344-5g | €283.20 |
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) | C16H27BO2S |
|---|---|
| CAS Number | 850881-09-3 |
| Molecular Weight | 294.26 |
| NACRES | NA.22 |
| PubChem Substance ID | 329761917 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD11045447 |
Safety Information Handling visibility
| Storage Class | 10 - Combustible liquids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | >230.0 °F |
| flash_point_c | > 110 °C |
| ppe | Eyeshields, Gloves, multi-purpose combination respirator cartridge (US) |
Technical Overview & Applications Use-case context
3-Hexylthiophene-2-boronic acid pinacol ester, with the CAS number 850881-09-3, is a crucial intermediate in the synthesis of various organic compounds, particularly in the field of materials science and organic electronics. This boronic ester is widely utilized in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of complex molecules with high efficiency and selectivity. The presence of the hexyl chain on the thiophene ring provides solubility and stability to the molecule, making it an attractive building block for the construction of conjugated polymers and oligomers. The pinacol ester moiety serves as a protective group, facilitating the handling and storage of the compound, and can be easily cleaved under basic conditions to reveal the boronic acid functionality, enabling further chemical transformations and applications in the development of novel materials.
