Ordering
Available Variants250 mg
CHA.18610-250mg
Price
€88.00
Available – Dispatch in 14 days
1 g
CHA.18610-1g
Price
€138.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
250 mg | CHA.18610-250mg | €88.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.18610-1g | €138.40 |
≥95.0%
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) | C3H5BN2O2 |
|---|---|
| CAS Number | 763120-58-7 |
| Molecular Weight | 111.90 |
| NACRES | NA.22 |
| PubChem Substance ID | 329762624 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD07368251 |
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 |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
1H-Pyrazole-4-boronic acid, with the CAS registry number 763120-58-7, is a boronic acid derivative of pyrazole, exhibiting a range of applications in organic synthesis and medicinal chemistry. This compound serves as a versatile building block for the construction of complex molecules, including pharmaceuticals and agrochemicals. The boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds with various aryl and vinyl partners. As a result, 1H-pyrazole-4-boronic acid has been utilized in the synthesis of numerous biologically active compounds, including kinase inhibitors and other therapeutically relevant molecules. Its unique combination of reactivity and stability makes it a valuable intermediate in modern organic synthesis, contributing to the development of new chemical entities with potential applications in human health and agriculture.
