cas 571157-73-8|| where to buy 2-chloro-N-{4-methoxy-8-oxatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}propanamide

Nom du produit:2-chloro-N-{4-methoxy-8-oxatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}propanamide

IUPAC Name:2-chloro-N-{4-methoxy-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-5-yl}propanamide

Unité d'emballage	Stock disponible	Prix($)
CM480585-50mg	in stock	Ǫƈȃ
CM480585-100mg	in stock	ľƈŗ
CM480585-250mg	in stock	ƿƿȃ
CM480585-500mg	in stock	ŗĲǪ
CM480585-1g	in stock	ǙǙĲƿ
CM480585-5g	in stock	ľľƿƿ
CM480585-10g	in stock	ƿŹȃǪ

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: N° CAS:571157-73-8; Formule moléculaire:C16H14ClNO3; Point de fusion:-; Code SMILES:COC1=CC2=C(OC3=C2C=CC=C3)C=C1NC(=O)C(C)Cl; Densité:

: Numéro de catalogue:CM480585; Poids moléculaire:303.74; Point d'ébullition:; N° Mdl:MFCD03988567; Stockage:

: Dibenzofurans; Dibenzofuran is an organic compound (C12H8O) consisting of two benzene rings fused to a central furan ring. Dibenzofuran can be synthesized by annealing and oxidative coupling methods of diphenyl ether, biphenyl derivatives, benzofuran, quinone. Most of the dibenzofuran-related natural products are metabolites of lichens or higher fungi. Lichen dibenzofurans appear to be formed by carbon-carbon oxidative coupling of orsellinic acid and its homologs.