| Field | Specification |
|---|---|
| CAS no. | |
| Applications | |
| Source | Plant — Bignoniaceae Radermachera xylocarpa (Roxb.) Roxb. ex K.Schum. |
| Molecular weight | |
| Molecular formula | C24H16O4 |
| SMILES | |
| Storage | |
| Shipping | |
| Catalog no. (Mfr.) | |
| Main SKU |
Compound Overview
Radermachol is a red pigment that can be synthesized in four steps through a key ytterbium triflate-catalyzed furan cyclization followed by an intramolecular nucleophilic acylation reaction[1]. It is naturally sourced from the plant Radermachera xylocarpa (Bignoniaceae), with a molecular formula of C24H16O4 and a molecular weight of 368.38 g/mol.
Physical & Chemical Properties
| CAS Number | 95378-00-0 |
|---|---|
| Molecular Formula | C24H16O4 |
| Molecular Weight | 368.38 g/mol |
| Structure Classification | Others |
| SMILES | O=C1C2=CC=CC=C2C(C3=C4C(OC(/C=C(C)\C)=C41)=C(C=CC=C5)C5=C3O)=O |
| Initial Source | Plant — Bignoniaceae Radermachera xylocarpa (Roxb.) Roxb. ex K.Schum. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Shipping | Room temperature in continental US; may vary elsewhere. |
Literature Cited
Sources cited in this description. Peer-reviewed publications that used this product are listed under References.
[1]. A four-step total synthesis of radermachol
Safety
For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.
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