Ordering
Available Variants1 g
CHA.77600-1g
Price
€17.84
Available – Dispatch in 14 days
5 g
CHA.77600-5g
Price
€22.16
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.77600-1g | €17.84 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.77600-5g | €22.16 |
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
| Linear Formula | FC6H4SO2Cl |
|---|---|
| CAS Number | 701-27-9 |
| Molecular Weight | 194.61 |
| NACRES | NA.22 |
| PubChem Substance ID | 24877909 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00042286 |
| Assay | 97% |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H314 |
| pcodes | P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405 |
| Hazard Classifications | Eye Dam. 1 - Skin Corr. 1B |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
3-Fluorobenzenesulfonyl chloride, with a CAS number of 701-27-9, is a chemical compound that has been utilized in various applications, including pharmaceutical synthesis and organic chemistry research. This compound exhibits a molecular structure consisting of a benzene ring substituted with a fluorine atom and a sulfonyl chloride group. The presence of the fluorine atom imparts unique properties to the molecule, including altered reactivity and stability. As a sulfonyl chloride, 3-fluorobenzenesulfonyl chloride is highly reactive and can participate in nucleophilic substitution reactions, making it a valuable intermediate in the synthesis of complex molecules. Its reactivity and versatility have led to its use in the preparation of various sulfonamides, sulfonates, and other sulfur-containing compounds, which are essential in the development of new pharmaceuticals and materials.
