792935-82-1

Basic information

• Product Name: D-xylo-Hex-1-enitol, 1,6-anhydro-2-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)
• Synonyms: D-xylo-Hex-1-enitol, 1,6-anhydro-2-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)
• CAS NO: 792935-82-1
• Molecular Formula: C11H16O5
• Molecular Weight: 228.24174
• Product Categories: METHYL
• Mol File: 792935-82-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: D-xylo-Hex-1-enitol, 1,6-anhydro-2-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: D-xylo-Hex-1-enitol, 1,6-anhydro-2-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)(792935-82-1)
• EPA Substance Registry System: D-xylo-Hex-1-enitol, 1,6-anhydro-2-deoxy-3,4-O-(1-methylethylidene)-, acetate (9CI)(792935-82-1)

Safety Data

• Hazardous Substances Data: 792935-82-1(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 792935-90-1 (3R,4S,5R)-4,5-isopropylidenedioxy-2,3,4,5-tetrahydrooxepine-3-ol 
• 4099-88-1 (3aS,6R,6aS)-6-(hydroxymethyl)-2,2-dimethyl-tetrahydrofuro[3,4-d]-[1,3]dioxol-4-ol 
• 302553-89-5 (2R,3S,4R)-3,4-(isopropylidenedioxy)hex-5-yne-1,2-diol 
• 792935-83-2 (2S,3S,4S)-3,4-(isopropylidenedioxy)hex-5-yne-1,2-diol 
• 302554-14-9 (2R,3S,4S)-3,4-(isopropylidenedioxy)hex-5-yne-1,2-diol 
• 302554-11-6 (2R,3R,4S)-3,4-(isopropylidenedioxy)hex-5-yne-1,2-diol 

Relevant articles and documents

Fischer carbene catalysis of alkynol cycloisomerization: Application to the synthesis of the altromycin B disaccharide

The tungsten-catalyzed cycloisomerization of alkynyl alcohols can be conducted without using photochemistry, using a stable tungsten Fischer carbene as the precatalyst for this transformation. A variety of alkynyl alcohols undergo cycloisomerization under

Synthesis of seven-membered ring glycals via endo-selective alkynol cycloisomerization

Alkynyldiols 1 undergo cycloisomerization to the corresponding seven-membered cyclic enol ethers 2 under tungsten carbonyl catalysis. This novel transformation proceeds with good yields and virtually complete regioselectivity for all diastereomers of 1, f