112339-36-3

Usage

Uses

Used in Medicinal Chemistry:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, 4-methylbenzenesulfonate is used as a building block for the synthesis of new drugs and pharmaceutical compounds due to its unique structure and properties. The presence of the sulfonate group and the phenylmethyl group can alter the chemical and physical properties of the parent hexopyranose, making it a potentially useful compound for drug development.
Used in Drug Development:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, 4-methylbenzenesulfonate is used as a potential candidate for the development of new drugs. Its unique structure and properties, including the presence of the sulfonate group and the phenylmethyl group, can be exploited to create novel pharmaceutical compounds with improved therapeutic effects.
Used in Organic Synthesis:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, 4-methylbenzenesulfonate is used as a reagent in organic synthesis. Its unique structure and properties make it a valuable compound for the synthesis of various organic compounds and materials.
Used in Material Science:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, 4-methylbenzenesulfonate is used in material science for the development of new materials with specific properties. The presence of the sulfonate group and the phenylmethyl group can contribute to the creation of materials with unique characteristics, making it a potentially useful compound in this field.

Upstream product

• 112339-43-2 C₁₃H₁₆O₄ 
• 98-59-9 p-toluenesulfonyl chloride 
• 102719-11-9 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-arabino-hexopyranose 

Downstream Products

• 112339-07-8 1,6-anhydro-2-azido-4-O-benzyl-2,3-dideoxy-β-D-ribo-hexopyranose 

Relevant academic research and scientific papers

Synthesis of α-bromoisolevoglucosenone and its cyclopenta annulation

4,4-Dimethyl-3-nitro-10,11-dioxatricyclo[6.2.1.02,6]undec-5-en-7-one possessing a bicyclic iridoid skeleton was synthesized in two steps from isolevoglucosenone which was obtained in turn from levoglucosenone through 4-benzyloxy-2-tosyloxy deri

1,6-anhydro-β-hexopyranose derivatives and their use as herbicides and plant growth regulators

Herbicidal and/or plant-growth regulatory compositions comprising, together with a carrier and/or surface-active agent, an effective amount of at least one herbicidal and/or plant growth regulatory active agent selected from compounds of formula (I) STR1 (in which R represents an optionally substituted aralkyl group, X represents an O--, N-- or S-linked organic group, an optionally substituted hydrocarbyl group, a halogen atom, a hydroxy, amino, alkoxyamino, nitro, cyano, azido, sulpho or phospho group, or together with the group R2e, X may represents a ketonic oxygen atom --O-- or a group of formula --CH2 O--; R1e represents a hydrogen atom or an optionally substituted hydrocarbyl group, or a formyl group; R2e represents a hydrogen atom, a hydroxy group or an optionally substituted hydrocarbyl or O-linked hydrocarbyl group, or, together with the group X, R2e may represent a ketonic oxygen atom --O-- or a group of formula --CH2 O--; R3a represents a hydrogen atom, a hydroxy group or an optionally substituted alkoxy, alkenyloxy, aralkoxy or C1-4 hydrocarbyl group; R3e represents a hydrogen atom, a hydroxy group or an optionally substituted hydrocarbyl or O-linked hydrocarbyl group; and R4e represents a hydrogen atom or an optionally substituted hydrocarbyl group) and enantiomers and salts thereof. Methods for preparing the compounds of formula (I) are described; the compositions are valuable as herbicides and/or plant-growth regulants, particularly for use with crops such as soya, rape, sugar-beet, cotton, wheat, maize and rice.