Phendioxan

Phendioxan
Names
	Preferred IUPAC name 2-(2,6-Dimethoxyphenoxy)-N-{[(2R,3R)-3-phenyl-2,3-dihydro-1,4-benzodioxin-2-yl]methyl}ethan-1-amine
Identifiers
CAS Number	130905-04-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL287935;
ChemSpider	161227;
PubChem CID	185453;
UNII	9GA78MV6TU ;
CompTox Dashboard (EPA)	DTXSID50926963 ;
	InChI InChI=1S/C25H27NO5/c1-27-21-13-8-14-22(28-2)25(21)29-16-15-26-17-23-24(18-9-4-3-5-10-18)31-20-12-7-6-11-19(20)30-23/h3-14,23-24,26H,15-17H2,1-2H3/t23-,24-/m1/s1 Key: UVEKKXRFQCNLQE-DNQXCXABSA-N; InChI=1/C25H27NO5/c1-27-21-13-8-14-22(28-2)25(21)29-16-15-26-17-23-24(18-9-4-3-5-10-18)31-20-12-7-6-11-19(20)30-23/h3-14,23-24,26H,15-17H2,1-2H3/t23-,24-/m1/s1 Key: UVEKKXRFQCNLQE-DNQXCXABBD;
	SMILES COC1=C(C(=CC=C1)OC)OCCNC[C@@H]2[C@H](OC3=CC=CC=C3O2)C4=CC=CC=C4;
Properties
Chemical formula	C25H27NO5
Molar mass	421.493 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Phendioxan is an α₁-adrenergic receptor antagonist.^[1]

References

↑ Quaglia, W; Pigini, M; Tayebati, SK; Piergentili, A; Giannella, M; Marucci, G; Melchiorre, C (1993). "Structure-activity relationships in 1,4-benzodioxan-related compounds. 4. Effect of aryl and alkyl substituents at position 3 on alpha-adrenoreceptor blocking activity". Journal of Medicinal Chemistry. 36 (11): 1520–8. doi:10.1021/jm00063a002. PMID 8098772.

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