Ordering
Available Variants5 g
CHA.39665-5g
Price
€40.24
Available – Dispatch in 14 days
25 g
CHA.39665-25g
Price
€74.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.39665-5g | €40.24 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.39665-25g | €74.00 |
96%
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 | BrCH2COC6H4CN |
|---|---|
| CAS Number | 20099-89-2 |
| Molecular Weight | 224.05 |
| NACRES | NA.22 |
| PubChem Substance ID | 24878394 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00052931 |
| Assay | 96% |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
  GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H302 + H312 + H332,H314 |
| pcodes | P260 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B |
| Storage Class | 6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
2-Bromo-4-cyanoacetophenone, with the CAS registry number 20099-89-2, is a synthetic organic compound that has garnered significant attention in various chemical and pharmaceutical applications. This compound exhibits a unique combination of functional groups, including a bromo substituent and a cyano group, which impart distinct reactivity and properties. The presence of the acetophenone moiety further enhances its versatility, allowing it to participate in a range of chemical transformations. As a result, 2-Bromo-4-cyanoacetophenone has been employed as a key intermediate in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. Its chemical structure and properties make it an attractive starting material for the development of new compounds with potential biological activity, underscoring its importance in modern organic chemistry and drug discovery endeavors.
