2,3-O-Isopropylidene-D-erythronolactone TCI I0454

Chemical Identity

CAS No.: 25581-41-3
PubChem: CID 386843·SID 87571806
Formula: C7H10O4
Molecular weight: 158.15 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3aR,6aR)-2,2-dimethyl-6,6a-dihydro-3aH-furo[3,4-d][1,3]dioxol-4-one
SMILES: CC1(O[C@@H]2COC(=O)[C@@H]2O1)C
InChIKey: WHPSMBYLYRPVGU-RFZPGFLSSA-N

Rp 10.599.750,00

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2,3-O-Isopropylidene-D-erythronolactone is a chemical compound widely used in chemical and biochemical experiments, particularly in glycoscience research. It is a stable lactone ring structure that serves as a key intermediate in the synthesis of complex glycosidic compounds. This compound is essential in laboratory settings where precise chemical reactivity and stability are required. Its unique molecular structure enables it to act as a substrate or intermediate in various organic synthesis reactions, making it a versatile tool for researchers.

The compound’s chemical properties, including its isopropylidene group, provide both stability and reactivity, making it a preferred choice for controlled chemical reactions. Its resistance to degradation ensures consistent performance in experimental conditions, which is critical for reliable results. The molecular complexity of 2,3-O-Isopropylidene-D-erythronolactone allows it to participate in a wide range of synthetic pathways, supporting the development of bioactive compounds and pharmaceuticals. Its specificity and reliability make it a valuable asset in laboratory workflows.

In Indonesian laboratories, 2,3-O-Isopropylidene-D-erythronolactone is commonly used in biochemical, pharmacological, and organic chemistry research. Researchers rely on this compound for the synthesis of glycosidic compounds, drug development, and studies on biological activities. Its role in these applications underscores its importance in advancing scientific understanding and innovation in the field of chemistry.

TCI brochures (PDF)

Reagents for Glyco Chemistry & Biology 5th Edition · p. 14

Related TCI products

Biochemical research utilizes this compound for the synthesis of glycosidic structures due to its stable lactone ring and reactivity.
Pharmacological studies benefit from its role in the development of bioactive compounds through controlled chemical reactions.
Organic chemistry experiments leverage its molecular complexity to create new synthetic pathways and functional derivatives.
Drug development projects use it as a precursor for the synthesis of complex glycosidic molecules with therapeutic potential.
Glycoscience research employs it to study carbohydrate-based interactions and their biological functions in cellular processes.

Brand	TCI
CAS number	25581-41-3
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 stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to air and humidity. Proper labeling of storage containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. It should be kept in a well-ventilated area to ensure safe working conditions. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in experiments.

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