Ordering
Available Variants1 g
CHA.33704-1g
Price
€28.00
Available – Dispatch in 14 days
5 g
CHA.33704-5g
Price
€81.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.33704-1g | €28.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.33704-5g | €81.60 |
≥95%
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) | C8H9BO4 |
|---|---|
| CAS Number | 164014-95-3 |
| Molecular Weight | 179.97 |
| NACRES | NA.22 |
| PubChem Substance ID | 24882748 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD01009696 |
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 |
| flash_point_f | No data available |
| flash_point_c | No data available |
Technical Overview & Applications Use-case context
1,4-Benzodioxane-6-boronic acid, with a CAS number of 164014-95-3, is a boronic acid derivative of 1,4-benzodioxane. This compound is a versatile intermediate in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. The boronic acid functional group allows for the compound to participate in a wide range of reactions, making it a valuable building block in the synthesis of complex molecules. Its unique structure, featuring a 1,4-benzodioxane ring system, also makes it an attractive starting material for the preparation of biologically active compounds and materials with potential applications in fields such as pharmaceuticals and materials science. As a result, 1,4-benzodioxane-6-boronic acid has become an important reagent in modern organic synthesis.
