Kromano
| Kromano | |
|---|---|
| Formula kimikoa | C9H10O |
| SMILES kanonikoa | 2D eredua |
| MolView | 3D eredua |
| Mota | chromane (en) |
| Masa molekularra | 134,073 Da |
| Identifikatzaileak | |
| InChlKey | VZWXIQHBIQLMPN-UHFFFAOYSA-N |
| CAS zenbakia | 493-08-3 |
| ChemSpider | 120093 |
| PubChem | 136319 |
| Reaxys | 116150 |
| Gmelin | 33224 |
| ChEBI | 122981 |
| EC zenbakia | 874-955-4 |
| ECHA | 100.344.744 |
| Human Metabolome Database | HMDB0250202 |
| UNII | EJ8R7LY9PK |
Kromanoa konposatu organiko heteroziklikoa da C9H10O formula duena. Likido sukoia da. Narritagarria da[1].
Kromanoaren egitura konposatu kimiko garrantzitsutan ageri da hala, tokoferola, tokotrienolak eta nebibolol botikan.
Sintesia
Kromanoa eta bere deribatuak sintetizatzeko anitz prozedura seinalatzen dira literaturan[2]. Horrelako bat orto-(3-zetoalki)lfenolak sodio borhidruroz tratatuz abiatzen da hiru urratsetako prozesu bati jarraituz[3].
Erreferentziak
- ↑ (Ingelesez) PubChem. «Chroman» pubchem.ncbi.nlm.nih.gov (kontsulta data: 2026-05-17).
- ↑ head-to-head comparison of different chromane synthesis routes. Bench-Chem.
- ↑ Synthesis of chromans and flavanes. Organic Chemitry Portal.
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