Ordering
Available Variants250 mg
CHA.70883-250mg
Price
€57.68
Available – Dispatch in 14 days
1 g
CHA.70883-1g
Price
€219.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
250 mg | CHA.70883-250mg | €57.68 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.70883-1g | €219.20 |
95%
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) | C52H44N2O2P2 |
|---|---|
| CAS Number | 205495-66-5 |
| Molecular Weight | 790.87 |
| NACRES | NA.22 |
| PubChem Substance ID | 329761527 |
| UNSPSC Code | 12352005 |
| MDL number | MFCD02684552 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
The (S,S)-DACH-naphthyl Trost Ligand, with a CAS number of 205495-66-5, is a chiral ligand utilized in various asymmetric catalytic reactions. This ligand is particularly effective in promoting enantioselective transformations, such as asymmetric allylic alkylation reactions. Its structure, featuring a DACH backbone and naphthyl substituents, provides a unique steric and electronic environment that enables high levels of enantioinduction. The (S,S)-DACH-naphthyl Trost Ligand has been employed in the synthesis of complex molecules, including pharmaceuticals and natural products, where its ability to induce high enantioselectivity is crucial. As a result, this ligand has become a valuable tool in the field of asymmetric catalysis, allowing chemists to access a wide range of enantiomerically enriched compounds with high efficiency and selectivity. Its applications continue to expand, driven by the growing demand for enantiopure molecules.
