3-Bromobenzoyl Chloride TCI B0557

Chemical Identity

CAS No.: 1711-09-7
PubChem: CID 74377·SID 87563576
Formula: C7H4BrClO
Molecular weight: 219.46 g/mol
Purity: >98.0%(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromobenzoyl chloride
SMILES: C1=CC(=CC(=C1)Br)C(=O)Cl
InChIKey: PBOOZQFGWNZNQE-UHFFFAOYSA-N

Rp 980.700,00

~~Rp 701.400,00~~ Rp 980.700,00

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3-Bromobenzoyl Chloride is a chemical compound widely used as a foundational building block in the synthesis of complex organic molecules. It contains a bromo group and a benzoyl group attached to a chlorine atom, making it a versatile reagent in organic chemistry. In laboratory settings, this compound plays a crucial role in facilitating substitution reactions and the formation of new chemical bonds. Its unique structure allows it to participate in various reaction mechanisms, making it an essential tool for synthetic chemists.

The reactivity of 3-Bromobenzoyl Chloride, combined with its ability to form stable intermediates, makes it a preferred choice in many synthetic pathways. Its compatibility with a wide range of functional groups enables chemists to design and execute complex reactions with high efficiency. The compound's ability to engage in SN2, SN1, and electrophilic reactions further enhances its utility in organic synthesis. These properties make it a reliable and effective reagent for both academic and industrial research.

In Indonesian laboratories, 3-Bromobenzoyl Chloride is extensively used by researchers and educational institutions for the development of new compounds. It is a key component in the synthesis of pharmaceuticals, materials, and specialty chemicals. Its availability and reliability make it a popular choice for both basic and advanced research projects in the field of organic chemistry.

Related TCI products

Organic synthesis of pharmaceutical compounds due to its reactivity and ability to form stable intermediates.
Development of new materials through its participation in substitution and bond-forming reactions.
Research in chemical engineering for the production of specialty chemicals and industrial applications.
Educational use in academic institutions for teaching advanced organic chemistry techniques.
Investigation of reaction mechanisms in both academic and industrial research settings.

Brand	TCI
CAS number	1711-09-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from light and moisture

3-Bromobenzoyl Chloride should be stored in a cool, dry place, away from light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of materials compatible with its chemical nature, such as glass or high-density polyethylene. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment like gloves and safety goggles. Avoid exposure to heat and incompatible substances to prevent unwanted reactions. Always ensure proper ventilation in the workspace to minimize inhalation risks. Regularly check storage conditions to ensure the compound remains stable and safe for use in laboratory settings.

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