29973-19-1

Usage

Uses

Used in Pharmaceutical Industry:
6-(acetylamino)cyclohexane-1,2,3,4,5-pentayl pentaacetate is used as a pharmaceutical intermediate for the synthesis of various drugs and active pharmaceutical ingredients. Its complex structure and potential reactivity make it a promising candidate for the development of new therapeutic agents.
Used in Chemical Research:
6-(acetylamino)cyclohexane-1,2,3,4,5-pentayl pentaacetate is used as a research compound in chemical laboratories for studying its properties, reactivity, and potential applications in various chemical reactions and processes.
Used in Material Science:
6-(acetylamino)cyclohexane-1,2,3,4,5-pentayl pentaacetate may be used in the development of new materials with unique properties, such as polymers, coatings, or adhesives, due to its complex structure and potential reactivity.
Used in Analytical Chemistry:
6-(acetylamino)cyclohexane-1,2,3,4,5-pentayl pentaacetate can be employed as a reference compound or standard in analytical chemistry for the calibration of instruments and the development of new analytical methods.
Note: The specific applications mentioned above are hypothetical and provided as examples based on the complex structure and potential reactivity of 6-(acetylamino)cyclohexane-1,2,3,4,5-pentayl pentaacetate. Further studies and research are necessary to confirm its actual uses and properties.

Upstream product

• 108-24-7 acetic anhydride 
• 169529-93-5 (-)-2,3-dibromocyclohex-5-ene-1,4-diol 
• 80582-73-6 (1S,2R,3S,6S)-2-bromo-7-oxabicyclo[4.1.0]hept-4-en-3-ol 
• 251538-17-7 (1S,2R,3S,6R)-6-azido-2-bromocyclohex-4-ene-1,3-diol 
• 639079-42-8 (1R,2S,3S,4R)-1-azidoconduritol B 
• 488-53-9 (+/-)-6t-amino-cyclohexane-1r,2c,3c,4t,5c-pentaol 
• 488-53-9 (+/-)-6c-amino-cyclohexane-1r,2c,3c,4t,5c-pentaol 
• 31077-18-6 1,2,3,4,5,-penta-O-acetyl-6-bromo-6-deoxy-scyllo-inositol 
• 64288-00-2 trans-cyclohexa-3,5-diene-1,2-diyl diacetate 
• 78775-99-2 2-Oxa-3-azabicyclo<2.2.2>-5-octen-7-exo-8-endo-diyldiacetat-hydrochlorid 
• 639799-29-4 (-)-1,2,3,5,6-penta-O-acetyl-4-deoxy-4-azido-myo-inositol 
• 639079-54-2 (+)-1,5,6-tri-O-acetyl-4-azido-myo-inositol 
• 639799-16-9 (1R,2S,3S,4R)-2,3,4-tri-O-acetyl-1-azidoconduritol B 

Downstream Products

• 3613-86-3 (+/-)-2-acetylamino-2-deoxy-epi-inositol 

Relevant academic research and scientific papers

Stereoselective synthesis of several azido/amino- and diazido/diamino-myo-inositols and their phosphates from p-benzoquinone

A practical route is described for the preparation of azido-myo-inositols, amino-myo-inositols and azido-conduritol B derivatives. Starting from p-benzoquinone, optically pure compounds in both forms can be prepared via enzymatic resolution of a derived diacetoxy conduritol B derivative. Selective introduction of nitrogen-containing functional groups in four of the six possible positions in the cyclitol moiety is followed by further functionalization to yield the target compounds.

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, VI. - Syntheses of Inosamine Derivatives

With trans-6-methoxy-1,3-cyclohexadiene-5,6-diyldiacetate or -5,6-diol inosamine derivatives are synthesized in good yield.

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, VII. - Synthesis of Conduramine-F1

A two-step synthesis of conduramine-F1 with trans-1,3-cyclohexadien-5,6-diyldiacetat (1) as educt is described.

Synthetic Study and Conformational Analysis of O-Benzylated Aminocyclitols

DL-(1,3/2)-3-Acetamido-1,2-di-O-benzylcyclohex-4-enediol (IIIa) and DL-(1,3/4)-1-acetamido-3,4-di-O-benzylcyclohex-5-enediol (IIIb) were synthesized from DL-trans-1,2-di-O-benzylcyclohex-3-enediol (I) via the corresponding azide derivatives (IIa-b) prepar

Conversion of 1,6-Anhydromaltose into Pseudodisaccharides Containing Aminocyclitols as Constituent

1,6-Anhydromaltose was chemically converted into a couple of pseudodisaccharides containing different inosamine (3-amino-3-deoxy-epi- and 1-amino-1-deoxy-1 L-myo-inositol) residues as constituents via 6-deoxy-6-nitro-maltose derivatives.