1414125-76-0

Basic information

• Product Name: (E)-2-[3,4-bis(methoxymethoxy)styryl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: (E)-2-[3,4-bis(methoxymethoxy)styryl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 1414125-76-0
• Molecular Weight: 350.22
• Mol File: 1414125-76-0.mol

Chemical Properties

• CAS DataBase Reference: (E)-2-[3,4-bis(methoxymethoxy)styryl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-[3,4-bis(methoxymethoxy)styryl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1414125-76-0)
• EPA Substance Registry System: (E)-2-[3,4-bis(methoxymethoxy)styryl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1414125-76-0)

Safety Data

• Hazardous Substances Data: 1414125-76-0(Hazardous Substances Data)

Upstream product

• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1414125-62-4 (E)-4-(2-iodovinyl)-1,2-bis(methoxymethoxy)benzene 
• 6515-06-6 3,4-bis-methoxymethoxy-benzaldehyde 

Downstream Products

• 848190-46-5 5-[(E)-3,4-bis(methoxymethoxy)styryl]-2-[(E)-3,7-dimethylocta-2,6-dienyl]-1,3-bis(methoxymethoxy)benzene 

Relevant articles and documents

Palladium-catalyzed routes to geranylated or farnesylated phenolic stilbenes: Synthesis of pawhuskin C and schweinfurthin J

Starting from double MOM-protected phloroglucinol, the facile total syntheses of bioactive natural products pawhuskin C and schweinfurthin J were accomplished in good overall yields. The Heck, Stille, or Suzuki coupling reactions of two different electron