1377949-02-4

Basic information

• Product Name: 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-2,2-dimethyl-6-(phenylacetoxy)benzo[d][1,3]dioxol-5-yl butanoate
• Synonyms: 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-2,2-dimethyl-6-(phenylacetoxy)benzo[d][1,3]dioxol-5-yl butanoate
• CAS NO: 1377949-02-4
• Molecular Weight: 783.122
• Mol File: 1377949-02-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-2,2-dimethyl-6-(phenylacetoxy)benzo[d][1,3]dioxol-5-yl butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-2,2-dimethyl-6-(phenylacetoxy)benzo[d][1,3]dioxol-5-yl butanoate(1377949-02-4)
• EPA Substance Registry System: 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-2,2-dimethyl-6-(phenylacetoxy)benzo[d][1,3]dioxol-5-yl butanoate(1377949-02-4)

Safety Data

• Hazardous Substances Data: 1377949-02-4(Hazardous Substances Data)

Upstream product

• 73447-99-1 2,2-Dimethyl-5-hydroxybenzo[1,3]dioxole 
• 533-73-3 1,2,4-Trihydroxybenzene 
• 1377948-89-4 4,7-dibromo-5,6-bis-(methoxymethoxy)-2,2-dimethylbenzo[d][1,3]dioxole 
• 1377948-91-8 2,2-dimethylbenzo[d][1,3]dioxole-5,6-dione 
• 1377948-94-1 5,6-bis(methoxymethoxy)-2,2-dimethylbenzo[d][1,3]dioxole 
• 1377948-97-4 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-2,2-dimethylbenzo[d][1,3]dioxole-5,6-diol 
• 1377948-92-9 2,2-dimethylbenzo[d][1,3]dioxole-5,6-diol 
• 1377948-99-6 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-6-hydroxy-2,2-dimethylbenzo[d][1,3]dioxol-5-yl phenylacetate 
• 141-75-3 butyryl chloride 
• 1377948-96-3 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-2,2-dimethylbenzo[d][1,3]dioxole-5,6-dione 
• 1377948-87-2 4,7-bis[4-(tert-butyldimethylsilyloxy)phenyl]-5,6-bis(methoxymethoxy)-2,2-dimethylbenzo[d][1,3]dioxole 

Relevant articles and documents

Total synthesis of thelephantin O, vialinin A/Terrestrin A, and terrestrins B-D

The first total synthesis of natural, unsymmetrical 2′,3′- diacyloxy-p-terphenyls, thelephantin O (1) and terrestrins C and D (2 and 3, respectively), was achieved via a practical route which was also applicable to the synthesis of the symmetrical diesters vialinin A/terrestrin A (4) and terrestrin B (5). Compounds 1-5 exhibited cytotoxicity against cancer cells (HepG2 and Caco2) with IC50 values of 13.6-26.7 μmol/L.