79850-99-0

Basic information

• Product Name: 1-(2,6-Bis-methoxymethoxy-phenyl)-4-(2-methyl-[1,3]dioxolan-2-yl)-butan-1-ol
• Synonyms: 1-(2,6-Bis-methoxymethoxy-phenyl)-4-(2-methyl-[1,3]dioxolan-2-yl)-butan-1-ol
• CAS NO: 79850-99-0
• Molecular Weight: 356.416
• Mol File: 79850-99-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(2,6-Bis-methoxymethoxy-phenyl)-4-(2-methyl-[1,3]dioxolan-2-yl)-butan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,6-Bis-methoxymethoxy-phenyl)-4-(2-methyl-[1,3]dioxolan-2-yl)-butan-1-ol(79850-99-0)
• EPA Substance Registry System: 1-(2,6-Bis-methoxymethoxy-phenyl)-4-(2-methyl-[1,3]dioxolan-2-yl)-butan-1-ol(79850-99-0)

Safety Data

• Hazardous Substances Data: 79850-99-0(Hazardous Substances Data)

Upstream product

• 24400-75-7 ethylene-cetal de la bromo-5 pentanone-2 
• 79834-12-1 2,6-bis((2-methoxyethoxy)methoxy)benzaldehyde 
• 3884-71-7 bromo-5-pentanone-2 
• 108-46-3 recorcinol 
• 57234-29-4 1,3-bis(methoxymethyl)resorcinol 

Downstream Products

• 102-07-8 bis(diphenyl)urea 
• 116387-05-4 C₂₆H₃₀O₁₀ 
• 116387-07-6 5-(3,5-Bis-methoxymethoxy-benzoyl)-3-methoxymethoxy-9-methyl-8,13-dioxa-tricyclo[7.3.1.0^2,7]trideca-2⁽⁷⁾,3,5-triene-4-carbaldehyde 
• 116387-06-5 (3,5-Bis-methoxymethoxy-phenyl)-(4-hydroxymethyl-3-methoxymethoxy-9-methyl-8,13-dioxa-tricyclo[7.3.1.0^2,7]trideca-2⁽⁷⁾,3,5-trien-5-yl)-methanol 
• 116387-16-7 C₂₄H₂₆O₈ 
• 116387-03-2 5-(3,5-Dimethoxy-benzoyl)-3-methoxymethoxy-9-methyl-8,13-dioxa-tricyclo[7.3.1.0^2,7]trideca-2⁽⁷⁾,3,5-triene-4-carbaldehyde 
• 116387-02-1 (3,5-Dimethoxy-phenyl)-(4-hydroxymethyl-3-methoxymethoxy-9-methyl-8,13-dioxa-tricyclo[7.3.1.0^2,7]trideca-2⁽⁷⁾,3,5-trien-5-yl)-methanol 
• 116387-04-3 C₂₄H₂₆O₉ 
• 116387-01-0 3-Methoxymethoxy-9-methyl-8,13-dioxa-tricyclo[7.3.1.0^2,7]trideca-2⁽⁷⁾,3,5-triene-4-carboxylic acid phenylamide 

Relevant articles and documents

Methoxymethyl-Directed Aryl Metalation. A Total Synthesis of (+/-)-Averufin

A total synthesis of (+/-)-averufin, a central intermediate in aflatoxin biosynthesis, is described.The key steps of the synthesis involve the following: (1) the regiospecific coupling of the phthalide anion of 3b and the benzyne derived in situ from aryl