Ordering
Available Variants1 g
CHA.18702-1g
Price
€46.00
Available – Dispatch in 14 days
5 g
CHA.18702-5g
Price
€139.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.18702-1g | €46.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.18702-5g | €139.20 |
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) | C11H17BN2O2 |
|---|---|
| CAS Number | 827614-64-2 |
| Molecular Weight | 220.08 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883087 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD05663837 |
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 | 11 - Combustible Solids |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
2-Aminopyridine-5-boronic acid pinacol ester, with the CAS number 827614-64-2, is a versatile intermediate in organic synthesis. This compound is a derivative of pyridine, where the boronic acid moiety is protected as a pinacol ester, making it suitable for various cross-coupling reactions. The presence of the amino group at the 2-position allows for further functionalization, providing a handle for the introduction of additional substituents. This compound has been employed in the synthesis of complex molecules, including pharmaceuticals and materials. Its unique combination of functional groups makes it an attractive building block for the construction of heterocyclic compounds, and its reactivity has been explored in various chemical transformations, including Suzuki-Miyaura coupling reactions, to form carbon-carbon and carbon-heteroatom bonds.
