![(R)-1-[(SP)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine professional packaging visual](/images/bottle.jpg?v=1778374124)
CHA.25834
(R)-1-[(SP)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine
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Ordering
Available Variants100 mg
CHA.25834-100mg
Price
€83.20
Available – Dispatch in 14 days
500 mg
CHA.25834-500mg
Price
€373.60
Available – Dispatch in 14 days
1 g
CHA.25834-1g
Price
€476.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 mg | CHA.25834-100mg | €83.20 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.25834-500mg | €373.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.25834-1g | €476.00 |
≥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) | C32H40FeP2 |
|---|---|
| CAS Number | 155830-69-6 |
| Molecular Weight | 542.45 |
| NACRES | NA.22 |
| PubChem Substance ID | 24888987 |
| UNSPSC Code | 12352005 |
| MDL number | MFCD01074442 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
(R)-1-[(SP)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine, with the CAS registry number 155830-69-6, is a complex organometallic compound that has garnered significant attention in the field of asymmetric catalysis. This chiral ligand is characterized by its unique ferrocenyl backbone, which is functionalized with a diphenylphosphino group and a di-tert-butylphosphino moiety. The compounds stereocenter is situated at the ethyl bridge, allowing for the formation of a stable and rigid chiral environment. As a result, (R)-1-[(SP)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine has been employed as a ligand in various transition metal-catalyzed reactions, including hydrogenations and cross-coupling reactions, often exhibiting high levels of enantioselectivity and catalytic efficiency. Its applications in organic synthesis have been extensively explored, particularly in the production of enantiomerically pure compounds.
