Ordering
Available Variants1 g
CHA.70038-1g
Price
€38.04
Available – Dispatch in 14 days
5 g
CHA.70038-5g
Price
€243.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.70038-1g | €38.04 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.70038-5g | €243.20 |
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) | C15H18BNO2 |
|---|---|
| CAS Number | 406463-06-7 |
| Molecular Weight | 255.12 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883128 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD06411327 |
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 |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
6-Quinolineboronic acid pinacol ester, with the CAS number 406463-06-7, is a boronic ester compound that has gained significant attention in the field of organic synthesis. This compound is a versatile intermediate used in various cross-coupling reactions, such as Suzuki-Miyaura reactions, to form complex molecules. The pinacol ester moiety provides stability and ease of handling, making it a preferred choice among chemists. The quinoline ring system is a common motif in many biologically active compounds, and the incorporation of this boronic ester into such molecules can lead to the development of new pharmaceuticals and materials. As a result, 6-Quinolineboronic acid pinacol ester has become a valuable tool in modern organic synthesis, enabling the efficient construction of complex quinoline-based compounds. Its applications continue to expand, driving innovation in various fields of chemistry.
