2-(4-Bromobutyl)-1,3-dioxolane TCI B2128

Chemical Identity

CAS No.: 87227-41-6
PubChem: CID 13780200·SID 87564996
Formula: C7H13BrO2
Molecular weight: 209.08 g/mol
Purity: >95.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-(4-bromobutyl)-1,3-dioxolane
SMILES: C1COC(O1)CCCCBr
InChIKey: UQTZEBQZCBQLAN-UHFFFAOYSA-N

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2-(4-Bromobutyl)-1,3-dioxolane is a chemical compound widely used in organic synthesis reactions within laboratory settings. As a building block in the field of chemistry, it plays a crucial role in the development of more complex organic molecules. This compound is particularly valued for its structural versatility, allowing it to participate in various types of chemical reactions. Its presence in the laboratory is essential for researchers aiming to create new compounds or modify existing ones through synthetic pathways. Due to its chemical stability and controlled reactivity, it is a reliable choice for both academic and industrial research.

The compound's unique chemical properties, including its bromo group on the butyl chain and the 1,3-dioxolane ring structure, contribute to its effectiveness in organic synthesis. These features provide a balance between reactivity and stability, making it suitable for reactions that require moderate chemical activity. Its solubility in organic solvents further enhances its usability, as it simplifies handling and purification processes. These characteristics make it a preferred material for chemists working on complex molecular structures.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in academic institutions. It is a key component in the synthesis of various organic compounds, supporting both teaching and research activities. Its availability and reliability make it an essential reagent for students and researchers alike, facilitating the exploration of chemical reactions and molecular design.

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Organic synthesis reactions benefit from this compound's controlled reactivity and structural versatility, enabling the creation of complex molecules.
It is ideal for substitution reactions due to its bromo group, which can be easily replaced in synthetic pathways.
In coupling reactions, its 1,3-dioxolane structure provides stability while allowing for functional group modifications.
It supports addition reactions by offering a stable yet reactive platform for chemical transformations.
Its solubility in organic solvents makes it suitable for purification and separation processes in laboratory settings.

Brand	TCI
CAS number	87227-41-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various sizes as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent contamination and evaporation. Due to its chemical nature, it should be stored separately from incompatible substances such as strong oxidizers or acids. Always ensure proper ventilation in the laboratory when handling this material. Personal protective equipment, including gloves and safety goggles, should be worn to minimize exposure. Regular inspection of storage conditions is advised to maintain the integrity and safety of the compound.

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