4-Bromo-1-indanone TCI B3801

Chemical Identity

CAS No.: 15115-60-3
PubChem: CID 98713·SID 253659604
Formula: C9H7BrO
Molecular weight: 211.05 g/mol
Purity: >97.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-bromo-2,3-dihydroinden-1-one
SMILES: C1CC(=O)C2=C1C(=CC=C2)Br
InChIKey: UVVYFYLSZIMKMC-UHFFFAOYSA-N

Rp 822.150,00

~~Rp 590.100,00~~ Rp 822.150,00

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4-Bromo-1-indanone is a chemical compound widely used in organic synthesis reactions within laboratory settings. As a building block in chemical research, it plays a crucial role in the development of complex molecular structures. Its aromatic structure, combined with a bromo substituent at the fourth position, provides it with unique reactivity and versatility. This compound is particularly valuable for its ability to participate in various synthetic pathways, making it a key reagent in both academic and industrial research environments.

The chemical properties of 4-Bromo-1-indanone make it a preferred choice for chemists. Its stable molecular structure allows for controlled reactions under laboratory conditions, while its reactivity supports a wide range of synthetic transformations. The compound is well-suited for substitution and electrophilic reactions, enabling the synthesis of heterocyclic compounds and their derivatives. These characteristics contribute to its popularity among researchers working on organic chemistry and pharmaceutical synthesis.

In Indonesian laboratories, 4-Bromo-1-indanone is commonly used in organic chemistry research and the synthesis of pharmacological compounds. It is a practical and reliable material for educational institutions and research organizations focused on chemical innovation. Its availability and chemical stability make it a valuable asset in both teaching and applied research settings.

Related TCI products

Organic synthesis reactions benefit from 4-Bromo-1-indanone due to its reactivity and structural versatility, enabling the creation of complex molecules.
Pharmaceutical compound development often utilizes this compound as a key intermediate in the synthesis of bioactive molecules.
Heterocyclic compound synthesis relies on 4-Bromo-1-indanone as a foundational building block for creating ring structures with functional groups.
Teaching laboratories use this compound to demonstrate substitution and electrophilic reaction mechanisms in organic chemistry courses.
Research institutions incorporate 4-Bromo-1-indanone into studies involving Diels-Alder and Friedel-Crafts reactions for structural modifications.

Brand	TCI
CAS number	15115-60-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid, crystalline
Storage	Store in a cool, dry place away from light and moisture

4-Bromo-1-indanone should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air. Due to its brominated structure, it is important to handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the workspace. The compound should be stored away from incompatible substances, such as strong oxidizers, to prevent any potential chemical reactions. Regular inspection of storage conditions is advised to ensure the integrity of the material remains intact.

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