![(S)-α,α-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol trimethylsilyl ether molecular structure](/images/molecules/-s----bis-3-5-bis-trifluoromethyl-phenyl--2-pyrrolidinemethanol-trimethylsilyl-ether-848821-61-4.png)
Ordering
Available Variants1 g
CHA.99213-1g
Price
€640.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.99213-1g | €640.80 |
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) | C24H23F12NOSi |
|---|---|
| CAS Number | 848821-61-4 |
| Molecular Weight | 597.51 |
| NACRES | NA.22 |
| PubChem Substance ID | 24885347 |
| UNSPSC Code | 12352005 |
| MDL number | MFCD09750447 |
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 |
| flash_point_f | >230.0 °F - closed cup |
| flash_point_c | > 110 °C - closed cup |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
(S)-α,α-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol trimethylsilyl ether, with the CAS number 848821-61-4, is a complex organic compound that has garnered significant attention in the scientific community. This molecule features a pyrrolidine backbone, which is a five-membered ring containing nitrogen, and is substituted with two bulky 3,5-bis(trifluoromethyl)phenyl groups. The presence of these substituents imparts unique steric and electronic properties to the molecule. Additionally, the compound is protected as a trimethylsilyl ether, which is a common protecting group used in organic synthesis to prevent unwanted reactions at the hydroxyl group. The synthesis and applications of this compound are of interest to researchers in the fields of organic chemistry and pharmaceuticals, where it may serve as a valuable intermediate or building block.
