Methyl 4,6-O-Benzylidene-alpha-D-glucopyranoside TCI M1125

Chemical Identity

CAS No.: 3162-96-7
PubChem: CID 11822086·SID 87573089
Formula: C14H18O6
Molecular weight: 282.29 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (4aR,6S,7R,8R,8aS)-6-methoxy-2-phenyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol
SMILES: CO[C@@H]1[C@@H]([C@H]([C@H]2[C@H](O1)COC(O2)C3=CC=CC=C3)O)O
InChIKey: VVSWDMJYIDBTMV-BTZLDLHRSA-N

Rp 1.140.300,00

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Berat 5g 25g

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Methyl 4,6-O-Benzylidene-alpha-D-glucopyranoside is a chemical compound widely utilized in laboratory settings for its role in chemical biology and glycoscience research. This compound is a glycoside with a complex structure, making it a key component in the synthesis of various glycosidic compounds. Its importance lies in its ability to participate in molecular interactions that are essential for understanding biological systems. Due to its structural complexity, it is often used as a building block in the development of bioactive molecules, contributing to advancements in pharmaceutical and biochemical research.

The compound is valued for its chemical stability under specific conditions, which facilitates long-term storage and consistent performance in experimental processes. Its solubility varies depending on the solvent used, offering flexibility in experimental design. This adaptability makes it a preferred choice for researchers requiring precise and reliable results. Additionally, its molecular structure allows for controlled modifications, enhancing its utility in a wide range of laboratory applications.

In Indonesian laboratories, this compound is commonly used in academic and industrial research settings, particularly in institutions focused on chemical biology and pharmacology. Its presence supports ongoing studies aimed at developing new therapeutic agents and understanding molecular interactions. The compound’s versatility and reliability make it an essential tool for researchers in Indonesia seeking to advance their work in these fields.

TCI brochures (PDF)

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

Related TCI products

Glycoside Synthesis: This compound is ideal for synthesizing glycosidic derivatives due to its stable structure and reactivity.
Molecular Interaction Studies: Its complex molecular framework enables detailed investigations into molecular recognition and binding processes.
Antimicrobial Compound Development: It serves as a precursor in the creation of bioactive molecules with antimicrobial properties.
Biochemical Research: Its use in biochemical assays supports the study of enzyme activity and substrate interactions.
Pharmaceutical Research: It is frequently employed in drug development to explore potential therapeutic applications in medicinal chemistry.

Brand	TCI
CAS number	3162-96-7
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Glycoscience
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its integrity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its complex molecular structure, it is important to ensure that it is used in a controlled environment to maintain the accuracy and consistency of experimental results. Proper storage and handling practices are essential to ensure the compound remains effective and safe for use in research applications.

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