![(+)-2,2′-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline] molecular structure](/images/molecules/--2-2--isopropylidenebis-4r--4-phenyl-2-oxazoline--150529-93-4.png)
Ordering
Available Variants250 mg
CHA.37994-250mg
Price
€80.00
Available – Dispatch in 14 days
1 g
CHA.37994-1g
Price
€221.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
250 mg | CHA.37994-250mg | €80.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.37994-1g | €221.60 |
97%
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Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C21H22N2O2 |
|---|---|
| CAS Number | 150529-93-4 |
| Molecular Weight | 334.41 |
| UNSPSC Code | 12352005 |
| NACRES | NA.22 |
| PubChem Substance ID | 24865413 |
| MDL number | MFCD00192244 |
| Beilstein/REAXYS Number | 4266906 |
Safety Information Handling visibility
| pictograms |
GHS06
 GHS06
|
|---|---|
| signalword | Danger |
| hcodes | H301 + H311 + H331 |
| pcodes | P261 - P264 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311 |
| Hazard Classifications | Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral |
| Storage Class | 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
(+)-2,2′-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline] is a chiral ligand with the CAS registry number 150529-93-4, utilized in various asymmetric catalytic reactions. This compound exhibits a high degree of stereoselectivity, making it a valuable tool in the synthesis of complex molecules. Its structure consists of two oxazoline rings connected by an isopropylidene bridge, with a phenyl group attached to each oxazoline ring. The (4R) configuration of the oxazoline rings is crucial for the ligands ability to induce asymmetry in catalytic reactions. As a result, (+)-2,2′-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline] has been employed in numerous studies to facilitate enantioselective transformations, including cycloaddition reactions and hydrogenations, often yielding products with high optical purity. Its applications continue to expand in the field of organic synthesis.
