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Available Variants1 g
CHA.91490-1g
Price
€69.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.91490-1g | €69.00 |
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) | C4H5BrN2O |
|---|---|
| CAS Number | 33084-49-0 |
| Molecular Weight | 177.00 |
| NACRES | NA.22 |
| PubChem Substance ID | 329763916 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD09038913 |
| Assay | 97% |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302,H315,H319,H335 |
| pcodes | P261 - P264 - P270 - P301 + P312 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Oral - 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 |
Technical Overview & Applications Use-case context
5-Amino-4-bromo-3-methylisoxazole, with the CAS registry number 33084-49-0, is a synthetic organic compound belonging to the isoxazole class. This compound exhibits a molecular structure characterized by a five-membered ring containing a nitrogen atom, an oxygen atom, and a methyl group attached to the third carbon atom. The presence of an amino group at the fifth position and a bromine atom at the fourth position confers unique chemical properties to this molecule. As a result, 5-Amino-4-bromo-3-methylisoxazole has been utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, taking advantage of its reactivity and versatility in forming new chemical bonds. Its applications are further expanded by the possibility of modifying its functional groups to produce a wide range of derivatives with distinct biological activities.
