Ordering
Available Variants5 mg
CHA.63634-5mg
Price
€98.40
Available – Dispatch in 14 days
25 mg
CHA.63634-25mg
Price
€553.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mg | CHA.63634-5mg | €98.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 mg | CHA.63634-25mg | €553.60 |
≥98% (elemental analysis)
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) | C6H2FN3O3 |
|---|---|
| CAS Number | 29270-56-2 |
| Molecular Weight | 183.10 |
| UNSPSC Code | 12352100 |
| NACRES | NA.32 |
| PubChem Substance ID | 24894897 |
| MDL number | MFCD00010196 |
| Beilstein/REAXYS Number | 1077571 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319 |
| pcodes | P264 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 - P337 + P313 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | 235.4 °F - closed cup |
| flash_point_c | 113 °C - closed cup |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
4-Fluoro-7-nitrobenzofurazan, with the CAS registry number 29270-56-2, is a synthetic organic compound that has garnered significant attention in the realm of chemistry due to its unique structural and reactive properties. This compound belongs to the benzofurazan class, which is characterized by a fused ring system consisting of a benzene ring and a furazan ring. The incorporation of a fluorine atom at the 4-position and a nitro group at the 7-position confers distinct electronic and steric characteristics to the molecule, influencing its reactivity and potential applications. As a result, 4-fluoro-7-nitrobenzofurazan has been explored in various chemical transformations, including nucleophilic substitution and electrophilic aromatic substitution reactions, highlighting its versatility as a synthetic intermediate. Further research is warranted to fully elucidate the properties and potential uses of this intriguing compound.
