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Available Variants10 g
CHA.96671-10g
Price
€107.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 g | CHA.96671-10g | €107.20 |
Professionally catalogued chemical listing prepared to support identification, technical review, safety visibility, and structured B2B sourcing workflows.
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) | C14H10BBrO2 |
|---|---|
| CAS Number | 641144-16-3 |
| Molecular Weight | 300.94 |
| NACRES | NA.22 |
| PubChem Substance ID | 24881600 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD06411293 |
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 |
Technical Overview & Applications Use-case context
10-Bromoanthracene-9-boronic acid, with the CAS number 641144-16-3, is a boronic acid derivative of anthracene, which has been utilized in various organic synthesis reactions. This compound is particularly useful in Suzuki-Miyaura cross-coupling reactions, where it serves as a building block for the formation of complex aromatic molecules. The presence of the bromo substituent allows for further functionalization through other cross-coupling reactions, while the boronic acid moiety provides a handle for the introduction of various aryl or heteroaryl groups. As a result, 10-bromoanthracene-9-boronic acid has become a valuable intermediate in the synthesis of polycyclic aromatic hydrocarbons and other conjugated systems, which have potential applications in materials science and optoelectronics. Its unique combination of functional groups makes it a versatile tool for the construction of complex molecular architectures.
