334490-60-7

Upstream product

• 100-79-8 (R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol 
• 53380-10-2 1,3-bis((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)propan-2-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 196497-38-8 6-(benzyloxy)-4,8-dioxaundecane-1,2,10,11-tetraol 
• 338459-13-5 3,7,11,15,19-penta-O-benzyl-1,5,9,13,17-pentaoxacycloicosane-3,7,11,15,19-pentaol 
• 338459-11-3 3,7,11,15-tetra-O-benzyl-1,5,9,13-tetraoxacyclohexadecane-3,7,11,15-tetraol 
• 338459-07-7 2,6,10-tri-O-benzyl-4,8-dioxaundecane-1,2,6,10,11-pentaol 
• 338459-09-9 3,7,11-tri-O-benzyl-1,5,9-trioxacyclododecane-3,7,11-triol 
• 925932-33-8 C₅₇H₆₈O₁₃S 
• 925932-32-7 C₅₀H₆₂O₁₁ 
• 925932-31-6 C₄₇H₅₆O₁₁S 
• 925932-30-5 C₄₀H₅₀O₉ 
• 195131-80-7 C₃₆H₄₈O₉ 
• 925932-29-2 2,6,10-O-tribenzyl-1-O-(4-toluenesulfonyl)-4,8-dioxaundecane-1,2,6,10,11-pentaol 
• 925932-27-0 C₄₄H₅₀O₁₁S₂ 
• 925932-26-9 6-(benzyloxy)-1,11-bis(tert-butyldiphenylsiloxy)-4,8-dioxaundecane-2,10-diol 

Relevant academic research and scientific papers

Synthesis of structurally weil-defined triglyceryl di-, tri-, and tetra-fatty acid esters as new oil gelators

We are interested in developing chemically modified linear and cyclic polyglycerols and their esters that have a single polymerization degree and fine structure. Triglyceryl di-, tri-, and tetra-fatty acid esters were synthesized from common substrate as new prominent gelators. The triglyceryl esters were capable of gelling up cooking oils. A comparison of the gelation ability of structurally related compounds clarified that the introduction of alkyl chains of suitable length is required for effective gelation. Georg Thieme Verlag Stuttgart · New York.

Synthesis of cyclic polyglycerols

Authentic standards of cyclic polyglycerol, with well-defined structures and degrees of polymerization from 3 to 6 cyclic oligomers, have been efficiently synthesized. The intramolecular cyclization conditions gave cyclic glycerols more effectively than intermolecular coupling conditions.