28810-04-0 Usage
Chemical structure
A complex chemical compound consisting of multiple acetyl and hexopyranose groups.
Derivative
A derivative of hexopyranose, a type of carbohydrate.
Acetyl groups
Has multiple acetyl groups attached to it.
Laboratory research
Often used in laboratory research as a building block for synthesizing more complex molecules.
Pharmaceutical development
Utilized in pharmaceutical development for exploring potential medical applications.
Unique structure
Its unique structure makes it a useful tool for studying carbohydrate chemistry.
Applications
Potential use in the development of new drugs and therapies targeting carbohydrate-related diseases.
Solubility
Likely soluble in organic solvents such as chloroform, methanol, or acetone, due to the presence of acetyl groups.
Stability
May be sensitive to hydrolysis or decomposition under certain conditions, such as high temperatures or in the presence of water.
Purity
Requires careful synthesis and purification techniques to ensure a high degree of purity for research and development purposes.
Safety precautions
Should be handled with care, as it may be toxic or harmful if ingested, inhaled, or absorbed through the skin.
Storage
Should be stored in a cool, dry place, away from light and moisture, to maintain its stability and prevent degradation.
Analytical techniques
Techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and infrared (IR) spectroscopy can be used to analyze and confirm the structure of 1,2,3-tri-O-acetyl-6-deoxy-4-O-(2,3,4,6-tetra-O-acetylhexopyranosyl)hexopyranose.
Synthesis
The synthesis of 1,2,3-tri-O-acetyl-6-deoxy-4-O-(2,3,4,6-tetra-O-acetylhexopyranosyl)hexopyranose likely involves multiple steps, including the formation of the hexopyranose core, selective protection of hydroxyl groups, and subsequent acylation with acetyl groups.
Structural analysis
The compound's structure can be further analyzed and understood through the examination of its stereochemistry, conformational preferences, and interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 28810-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28810-04:
(7*2)+(6*8)+(5*8)+(4*1)+(3*0)+(2*0)+(1*4)=110
110 % 10 = 0
So 28810-04-0 is a valid CAS Registry Number.
28810-04-0Relevant academic research and scientific papers
Electrochemical characterisation of 6-iodomaltose, 6′-iodomaltose and 6-iodomaltotriose on a silver cathode and their one-pot electrochemical dimerisation to new mixed O/C maltotetraose and maltohexaose mimics
Alberti, Angelo,Macciantelli, Dante,Naggi, Annamaria,Urso, Elena,Torri, Giangiacomo,Vismara, Elena
experimental part, p. 8005 - 8014 (2010/03/31)
The electrochemical reduction on silver of peracetylated 6-iodo6-deoxy-β-maltose (2), 6-iodo-6-deoxy-β-maltotriose (3) and 6′-iodo-6′-deoxy-β-maltose (4) has been investigated by cyclic voltammetry and performed on a preparative scale, according to the st
