Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-alpha-D-glucopyranoside TCI M2013

Chemical Identity

CAS No.: 6748-91-0
PubChem: CID 44629977·SID 87561032
Formula: C28H26O8
Molecular weight: 490.5 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(4aS,6S,7S,8S,8aR)-7-benzoyloxy-6-methoxy-2-phenyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-8-yl] benzoate
SMILES: CO[C@@H]1[C@H]([C@H]([C@H]2[C@@H](O1)COC(O2)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5
InChIKey: CGMUHSNJRXPSSA-VBBSJTGDSA-N

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Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-alpha-D-glucopyranoside is a complex chemical compound used in laboratory research related to glycoscience and biochemical studies. This compound is derived from glucose and modified with benzoyl and benzylidene groups, making it a valuable tool in molecular modification and structural analysis. Its unique structure allows it to serve as a substrate or reagent in various chemical reactions, particularly those involving glycosidic bond formation and modification. Due to its chemical stability under controlled conditions, it is widely used in high-precision laboratory environments where accuracy and consistency are essential.

The compound’s chemical properties, including its stability and defined molecular structure, make it a preferred choice for researchers working in glycoscience and chemical biology. Its high purity ensures reliable results in experiments requiring reproducibility and precision. The presence of multiple functional groups also allows for versatile chemical transformations, making it suitable for a wide range of synthetic and analytical applications. These characteristics make it an essential component in both academic and industrial research settings.

In Indonesian laboratories, this compound is commonly used in research related to glycoscience, particularly in pharmaceutical and biotechnology fields. Researchers in Indonesia frequently utilize it for studies involving molecular interactions, drug development, and biochemical pathway analysis. Its availability through suppliers like AMI Scientific ensures that Indonesian scientists have access to high-quality materials for their research needs.

TCI brochures (PDF)

Reagents for Glyco Chemistry & Biology 5th Edition · p. 35

Related TCI products

Glycoscience Research – This compound is ideal for studying glycosidic bond formation and modification due to its complex structure and functional groups.
Biochemical Analysis – Its stability and defined molecular structure make it suitable for use in biochemical assays and molecular interaction studies.
Pharmaceutical Development – It is used as a building block in the synthesis of glycoside-based compounds for drug development and therapeutic research.
Structural Chemistry Studies – The compound’s unique molecular architecture supports investigations into structural modifications and chemical reactivity.
Synthetic Organic Chemistry – Its reactivity and functional groups make it a valuable reagent in the synthesis of complex organic molecules.

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Brand – TCI
CAS Number – 6748-91-0
Category – Chemistry > Chemical Biology > Glycoscience
Pack Sizes – Available in various quantities as per supplier specifications
Physical Form – Solid powder
Storage Note – Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain its chemical integrity. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid contamination. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Always follow standard laboratory safety protocols when working with this compound to ensure a safe and controlled environment.

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