854936-82-6

Basic information

• Product Name: 1-bromomethyl-4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzene
• Synonyms: 1-bromomethyl-4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzene
• CAS NO: 854936-82-6
• Molecular Weight: 780.11
• Mol File: 854936-82-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-bromomethyl-4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromomethyl-4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzene(854936-82-6)
• EPA Substance Registry System: 1-bromomethyl-4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzene(854936-82-6)

Safety Data

• Hazardous Substances Data: 854936-82-6(Hazardous Substances Data)

Upstream product

• 623-24-5 1,4-bis(bromomethyl)benzene 
• 18794-74-6 1,3-bis(octadecyloxy)-2-propanol 
• 16245-97-9 octadecyl glycidyl ether 
• 112-92-5 1-octadecanol 

Downstream Products

• 854936-89-3 phenoxy-acetic acid 7-{2,3-dimethoxy-2,3,5-trimethyl-7-[4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzyloxy]-hexahydro-pyrano[3,4-b][1,4]dioxin-8-yloxy}-2,3-dimethoxy-2,3,5-trimethyl-hexahydro-pyrano[3,4-b][1,4]dioxin-8-yl ester 
• 854936-94-0 7-{2,3-dimethoxy-2,3,5-trimethyl-7-[4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzyloxy]-hexahydro-pyrano[3,4-b][1,4]dioxin-8-yloxy}-2,3-dimethoxy-2,3,5-trimethyl-hexahydro-pyrano[3,4-b][1,4]dioxin-8-ol 
• 854936-88-2 Phenoxy-acetic acid (2R,3R,4aS,5S,7R,8R,8aR)-2,3-dimethoxy-2,3,5-trimethyl-7-[4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzyloxy]-hexahydro-pyrano[3,4-b][1,4]dioxin-8-yl ester 
• 854936-93-9 (2R,3R,4aS,5S,7R,8R,8aS)-2,3-Dimethoxy-2,3,5-trimethyl-7-[4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzyloxy]-hexahydro-pyrano[3,4-b][1,4]dioxin-8-ol 
• 854936-84-8 [4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-phenyl]-methanol 
• 854936-83-7 acetic acid 4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzyl ester 

Relevant articles and documents

Efficient assembly of oligomannosides using the hydrophobically assisted switching phase method

The hydrophobically assisted switching phase (HASP) method was applied in the assembly of oligomannosides. A new mannosyl donor with high reactivity was selected after a series of optimization studies, which was suitable for the synthesis of oligomannosides via the HASP method. The practicability of the HASP method towards the synthesis of branched oligosaccharides was explored and two branched penta-mannosides were assembled efficiently.