製品名:4,6-Bis((S)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)dibenzo[b,d]furan

IUPAC Name:(4S)-4-tert-butyl-2-{10-[(4S)-4-tert-butyl-4,5-dihydro-1,3-oxazol-2-yl]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-6-yl}-4,5-dihydro-1,3-oxazole

CAS番号:2067322-25-0
分子式:C26H30N2O3
純度:95%+
カタログ番号:CM875155
分子量:418.54

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製品詳細

CAS番号:2067322-25-0
分子式:C26H30N2O3
融点:-
SMILESコード:CC(C)(C)[C@H]1COC(=N1)C1=CC=CC2=C1OC1=C2C=CC=C1C1=N[C@H](CO1)C(C)(C)C
密度:
カタログ番号:CM875155
分子量:418.54
沸点:
MDL番号:
保管方法:

Category Infos

Oxazolines
Oxazolines are five-membered heterocyclic compounds with one double bond. The double bond may be in one of three positions, so there may be three different oxazoline rings. The 2-oxazoline structure is the most common, and 3-oxazoline and 4-oxazoline exist mainly as laboratory research compounds. Oxazolines exist between oxazole and oxazolidine in terms of saturation.
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.

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