![(4S)-(+)-Phenyl-α-[(4S)-phenyloxazolidin-2-ylidene]-2-oxazoline-2-acetonitrile molecular structure](/images/molecules/-4s----phenyl----4s--phenyloxazolidin-2-ylidene--2-oxazoline-2-acetonitrile-150639-33-1.png)
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Available Variants1 g
CHA.65772-1g
Price
€394.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.65772-1g | €394.40 |
97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
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Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C20H17N3O2 |
|---|---|
| CAS Number | 150639-33-1 |
| Molecular Weight | 331.37 |
| NACRES | NA.22 |
| PubChem Substance ID | 24866118 |
| UNSPSC Code | 12352005 |
| MDL number | MFCD00192394 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
(4S)-(+)-Phenyl-α-[(4S)-phenyloxazolidin-2-ylidene]-2-oxazoline-2-acetonitrile, with the CAS registry number 150639-33-1, is a chiral auxiliary used in asymmetric synthesis. This compound is a key intermediate in the preparation of various enantiopure molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a phenyloxazolidin-2-ylidene moiety, allows it to participate in stereoselective reactions, such as aldol condensations and cycloadditions. The presence of the nitrile group also provides a convenient handle for further functionalization. As a result, this compound has found applications in the synthesis of complex molecules with high optical purity, making it a valuable tool in the field of organic chemistry. Its properties and reactivity have been extensively studied, and it continues to be a subject of interest in modern synthetic organic chemistry.
