CHA.88467
rac-BINAP Pd G4
--
--
Ordering
Available Variants250 mg
CHA.88467-250mg
Price
€85.80
Available – Dispatch in 14 days
1 g
CHA.88467-1g
Price
€341.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
250 mg | CHA.88467-250mg | €85.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.88467-1g | €341.60 |
powder
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) | C58H47NO3P2PdS |
|---|---|
| CAS Number | 1599466-90-6 |
| Molecular Weight | 1006.43 |
| MDL number | MFCD31707673 |
| UNSPSC Code | 12161600 |
| PubChem Substance ID | 329769806 |
| NACRES | NA.22 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|
Technical Overview & Applications Use-case context
rac-BINAP Pd G4, also known by its CAS number 1599466-90-6, is a palladium-based catalyst utilized in various asymmetric hydrogenation reactions. This complex features a BINAP ligand, which is a chiral diphosphine, and is often employed in the synthesis of enantiomerically enriched compounds. The palladium center in rac-BINAP Pd G4 enables efficient hydrogenation of unsaturated substrates, including alkenes and alkynes, under mild conditions. The catalysts activity and selectivity can be fine-tuned by adjusting reaction parameters, such as temperature, pressure, and solvent. rac-BINAP Pd G4 has been applied in the synthesis of pharmaceuticals, agrochemicals, and other valuable compounds, showcasing its versatility and potential in asymmetric catalysis. Its use has contributed significantly to the development of more efficient and sustainable synthetic methodologies in organic chemistry.
