3-Bromo-6-chlorochromone TCI B4967

Chemical Identity

CAS No.: 73220-38-9
PubChem: CID 3498945·SID 354334524
Formula: C9H4BrClO2
Molecular weight: 259.48 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromo-6-chlorochromen-4-one
SMILES: C1=CC2=C(C=C1Cl)C(=O)C(=CO2)Br
InChIKey: ZILSBPAUJJBEFF-UHFFFAOYSA-N

Rp 1.483.650,00

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3-Bromo-6-chlorochromone is a versatile chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds. As a building block in organic chemistry, it plays a crucial role in the development of complex molecules with specific biological activities. Its unique structure, featuring both bromo and chloro substituents, makes it an essential tool for researchers aiming to create compounds with tailored properties. This compound is particularly valuable in pharmaceutical and medicinal chemistry due to its reactivity and functional group versatility.

The reactivity of 3-Bromo-6-chlorochromone is largely attributed to its chromone core and the presence of halogen atoms. These groups serve as reactive sites for various chemical transformations, including electrophilic substitution, nucleophilic attack, and oxidation reactions. The compound's ability to participate in reactions such as Diels-Alder and nucleophilic substitution makes it highly sought after in synthetic chemistry. Its chemical stability under controlled conditions further enhances its utility in laboratory applications.

In Indonesian laboratories, 3-Bromo-6-chlorochromone is commonly used in scientific research and drug development projects. It is a key reagent in the synthesis of bioactive compounds, supporting both academic and industrial research efforts. Institutions and research centers in Indonesia rely on this compound for its reliability and effectiveness in creating complex molecular structures with potential therapeutic applications.

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive chromone core and halogen substituents.
Development of pharmaceuticals and bioactive molecules through nucleophilic and electrophilic substitution reactions.
Research in medicinal chemistry for the creation of compounds with targeted biological activities.
Use in academic laboratories for teaching and experimental research in synthetic organic chemistry.
Support for drug discovery initiatives by enabling the synthesis of complex molecular frameworks.

Brand	TCI
CAS number	73220-38-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

3-Bromo-6-chlorochromone should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled in a well-ventilated laboratory environment, preferably with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong bases or oxidizing agents. Always follow standard laboratory safety protocols when working with this compound to ensure safe and effective use.

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