1616345-57-3

Basic information

• Product Name: 1-O-{4-(trans-4-butylcyclohexyl)benzoyl}-2,3,4,6-tetra-O-methyl-β-D-glucopyranose
• Synonyms: 1-O-{4-(trans-4-butylcyclohexyl)benzoyl}-2,3,4,6-tetra-O-methyl-β-D-glucopyranose
• CAS NO: 1616345-57-3
• Molecular Weight: 478.626
• Mol File: 1616345-57-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-O-{4-(trans-4-butylcyclohexyl)benzoyl}-2,3,4,6-tetra-O-methyl-β-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-{4-(trans-4-butylcyclohexyl)benzoyl}-2,3,4,6-tetra-O-methyl-β-D-glucopyranose(1616345-57-3)
• EPA Substance Registry System: 1-O-{4-(trans-4-butylcyclohexyl)benzoyl}-2,3,4,6-tetra-O-methyl-β-D-glucopyranose(1616345-57-3)

Safety Data

• Hazardous Substances Data: 1616345-57-3(Hazardous Substances Data)

Upstream product

• 1139-97-5 2,3,4,6-tetra-O-methyl-D-glucopyranose 
• 83626-35-1 p-(4-trans-butylcyclohexyl)benzoic acid 

Relevant articles and documents

Synthesis of chiral dopants based on carbohydrates

Chiral dopants based on carbohydrates for nematic liquid crystals were synthesized from d-glucose, and their helical twisting power (HTP) values were evaluated. The chiral dopants induced helices in the host nematic liquid crystals. An acetyl derivative having an ether-type glycosidic linkage between carbohydrate and a mesogenic moiety showed the highest HTP value of 10.4 μm-1, while an acetyl derivative having an anomeric ester-type linkage did not show any HTP. It was surprising that this molecule had no HTP despite the presence of chirality in the molecule. A relationship between HTP and specific rotation was not observed in this study.