143573-26-6

Basic information

• Product Name: (1S,5R,6R,8R)-5-<(1R)-1,2-Dihydroxyethyl>-8-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane
• Synonyms: (1S,5R,6R,8R)-5-<(1R)-1,2-Dihydroxyethyl>-8-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane
• CAS NO: 143573-26-6
• Molecular Weight: 282.293
• Mol File: 143573-26-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1S,5R,6R,8R)-5-<(1R)-1,2-Dihydroxyethyl>-8-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,5R,6R,8R)-5-<(1R)-1,2-Dihydroxyethyl>-8-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane(143573-26-6)
• EPA Substance Registry System: (1S,5R,6R,8R)-5-<(1R)-1,2-Dihydroxyethyl>-8-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane(143573-26-6)

Safety Data

• Hazardous Substances Data: 143573-26-6(Hazardous Substances Data)

Upstream product

• 3530-21-0 (1S,5R,6R)-5-<(4R)-1,3-dioxolan-4-yl>-2,4,7,9-tetraoxabicyclo<4.4.0>decane 
• 3013-59-0 (4R,5R,6S)-4-<(1R)-1,2-Dihydroxyethyl>-5-hydroxy-6-hydroxymethyl-1,3-dioxane 
• 143573-25-5 (1S,5R,6R,8R)-5-<(4R)-2-Phenyl-1,3-dioxolan-4-yl>-8-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane 

Downstream Products

• 145260-14-6 1,3-bis(1,2-dideoxy-4,6-O-phenylmethylene-3,5-O-methylene-L-xylo-hex-1-enitolyl)-benzene, Z,E-isomer 
• 145260-14-6 1,3-bis((Z)-1,2-dideoxy-4,6-O-phenylmethylene-3,5-O-methylene-L-xylo-hex-1-enitolyl)-benzene 
• 145260-08-8 (4R,8S,21S,25R,33S,34S)-33,34-di(phenylmethoxy)-5,7,10,13,16,19,22,24-octaoxatetracyclo<26.3.1.1^4,8.1^21,25>tetratriaconta-1(32),28,30-triene 
• 145260-15-7 1,3-bis(1,2-dideoxy-4,6-O-phenylmethylene-3,5-O-methylene-L-xylo-hexitolyl)-benzene 
• 145260-16-8 1,3-bis(1,2-dideoxy-4-O-phenylmethyl-3,5-O-methylene-L-xylo-hexitolyl)-benzene 
• 143573-23-3 (1S,5S,6R,8R)-8-Phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane-5-carboxaldehyde 

Relevant articles and documents

Synthesis of carbohydrate containing crown ethers and their application as catalysts in asymmetric Michael additions

Synthesis of carbohydrate containing crown ethers tuned with steric and micro-environmental features and thier application as catalysts in the Michael addition of methyl phenylacetate to methyl acrylate to give a chiral products is reported. The mechanistic rationale of the asymmetric induction is discussed.