4891-18-3

Usage

Uses

Used in Pharmaceutical Industry:
(2-methoxy-3,6-dioxabicyclo[3.1.0]hex-4-yl)methanol is used as a solvent for the production of pharmaceuticals due to its ability to dissolve a wide range of substances and facilitate chemical reactions.
Used in Organic Synthesis:
In the field of organic synthesis, (2-methoxy-3,6-dioxabicyclo[3.1.0]hex-4-yl)methanol is used as a solvent to promote the formation of desired products and improve the efficiency of reactions.
While the compound is considered to have relatively low toxicity and is not classified as highly hazardous to human health or the environment, it is essential to adhere to proper handling and storage procedures to mitigate any potential risks associated with its use.

InChI:InChI=1/C6H10O4/c1-8-6-5-4(10-5)3(2-7)9-6/h3-7H,2H2,1H3

Upstream product

• 67-56-1 methanol 
• 124-41-4 sodium methylate 
• 110337-20-7 methyl-[O³-methanesulfonyl-O⁵-methoxycarbonyl-ξ-D-xylofuranoside 
• 109454-69-5 methyl-[O⁵-methoxycarbonyl-O³-(toluene-4-sulfonyl)-ξ-D-xylofuranoside 
• 1824-97-1 methyl β-D-xylofuranoside 
• 79083-42-4 methyl D-arabinofuranoside 
• 58-86-6 D-xylose 

Downstream Products

• 5467-30-1 methyl-(S-ethyl-3-thio-β-D-xylofuranoside) 
• 64623-01-4 methyl-[O⁵-(4-nitro-benzoyl)-2,3-anhydro-β-D-ribofuranoside] 
• 143604-34-6 5-O-Benzyl-3-chloro-2,3-didesoxy-2-dimethylamino-β-D-arabinofuranoside de methyle 
• 143604-33-5 5-O-Benzyl-2-chloro-2,3-didesoxy-3-dimethylamino-β-D-xylofuranoside de methyle 
• 143604-53-9 Methanesulfonate(1R,2S,4R,5S)-2-benzyloxymethyl-4-methoxy-6,6-dimethyl-3-oxa-6-azonia-bicyclo[3.1.0]hexane; 
• 60019-10-5 3-Amino-5-O-benzyl-3-desoxy-β-D-xylofuranoside de methyle 
• 143604-32-4 2-Amino-5-O-benzyl-2-desoxy-β-D-arabinofuranoside de methyle 
• 143604-38-0 5-O-Benzyl-2-desoxy-2-dimethylamino-β-D-arabinofuranoside de methyle 
• 143604-55-1 5-O-Benzyl-2,3-didesoxy-2-dimethylamino-3-fluoro-β-D-arabinofuranoside de methyle 
• 143604-36-8 5-O-Benzyl-3-desoxy-3-dimethylamino-β-D-xylofuranoside de methyle 
• 143604-54-0 5-O-Benzyl-2,3-didesoxy-3-dimethylamino-2-fluoro-β-D-xylofuranoside de methyle 
• 143604-43-7 5-O-Benzyl-3-desoxy-3-dimethylamino-2-O-methanesulfonyl-β-D-xylofuranoside de methyle 
• 143604-45-9 5-O-Benzyl-2-desoxy-2-dimethylamino-3-O-methanesulfonyl-β-D-arabinofuranoside de methyle 
• 113091-75-1 methyl-[S-ethyl-bis-O-(4-nitro-benzoyl)-3-thio-β-D-xylofuranoside] 

Relevant academic research and scientific papers

An efficient synthesis of methyl 2,3-anhydro-α-D-ribofuranoside

An efficient synthesis of methyl 2,3-anhydro-α-D-ribofuranoside is reported. Its preparation is achieved via a four-step sequence from methyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranoside in 74% overall yield.

Preparation of methyl 2,3-anhydro- and 2,3-o-sulfinylfuranosides from unprotected furanosides using the Mitsunobu reaction

A new two step procedure for the synthesis of methyl 2,3-anhydro-α-D-lyxofuranoside and methyl 2,3-anhydro-β-D-ribofuranoside from D-xylose involving the intramolecular Mitsunobu reaction is presented. Likewise, methyl 2,3-anhydro-α-L-lyxofuranoside is obtained from L-arabinose. Cyclic sulfites with D-ribo configuration, synthetic equivalents of the corresponding anhydrosugars, are prepared in three steps from D-ribose.