Ordering
Available Variants1 g
CHA.58939-1g
Price
€212.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.58939-1g | €212.00 |
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) | C12H21BO2 |
|---|---|
| CAS Number | 141091-37-4 |
| Molecular Weight | 208.10 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883742 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD05663845 |
Safety Information Handling visibility
| Storage Class | 10 - Combustible liquids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | 219.0 °F |
| flash_point_c | 103.9 °C |
| ppe | Eyeshields, Gloves, multi-purpose combination respirator cartridge (US) |
Technical Overview & Applications Use-case context
1-Cyclohexen-1-yl-boronic acid pinacol ester, with the CAS number 141091-37-4, is a versatile organoboronic ester compound that has gained significant attention in the field of organic synthesis. This compound is widely utilized as a building block in various cross-coupling reactions, such as Suzuki-Miyaura coupling, to form complex molecules. The presence of the pinacol ester group enhances the stability and reactivity of the boronic acid moiety, making it an ideal intermediate for the synthesis of pharmaceuticals, agrochemicals, and materials science applications. The compounds unique properties and reactivity profile have led to its increasing demand in research and development, particularly in the synthesis of cyclic and heterocyclic compounds, highlighting its importance as a valuable tool in modern organic chemistry. Its applications continue to expand, driven by ongoing research and advancements in synthetic methodologies.
