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Available Variants1 g
CHA.47748-1g
Price
€340.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.47748-1g | €340.80 |
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) | C18H19BO2S3 |
|---|---|
| CAS Number | 849062-17-5 |
| Molecular Weight | 374.35 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883379 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD06798103 |
| Assay | 96% |
| Form | solid |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
2,2′:5′,2″-Terthiophene-5-boronic acid pinacol ester, with the CAS number 849062-17-5, is a crucial intermediate in organic synthesis, particularly in the development of conjugated materials and organic electronics. This compound is a terthiophene derivative, consisting of three thiophene rings connected in a specific manner, and features a boronic acid pinacol ester moiety, which is widely used in Suzuki-Miyaura cross-coupling reactions. The presence of the boronic ester group allows for efficient and selective formation of carbon-carbon bonds, making this compound a valuable building block for the synthesis of complex molecules, including polythiophenes and other conjugated polymers. Its unique structure and reactivity render it an important tool in the design and synthesis of materials with tailored optical and electronic properties.
