2-Bromobenzaldehyde TCI B0836

Chemical Identity

CAS No.: 6630-33-7
PubChem: CID 81129·SID 87563820
Formula: C7H5BrO
Molecular weight: 185.02 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromobenzaldehyde
SMILES: C1=CC=C(C(=C1)C=O)Br
InChIKey: NDOPHXWIAZIXPR-UHFFFAOYSA-N

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2-Bromobenzaldehyde is a versatile organic compound widely used in laboratory settings for the synthesis of complex molecules. As a building block in chemical reactions, it serves as a key intermediate in the creation of aromatic and heterocyclic compounds. Its reactivity and ability to participate in various functional group interactions make it an essential tool for chemists. This compound is commonly found in both academic and industrial research laboratories, where it is used to develop new materials and pharmaceutical compounds. Its role in organic synthesis is critical due to its ability to act as both an electron donor and a substrate in substitution reactions.

The chemical properties of 2-Bromobenzaldehyde, including its reactivity and functional group versatility, make it a preferred choice for a wide range of synthetic applications. Its bromine substituent enhances its reactivity, allowing it to participate in nucleophilic substitution and coupling reactions. Additionally, its aldehyde group provides opportunities for further functionalization, making it a valuable reagent in the synthesis of more complex structures. These characteristics make it a go-to compound for researchers aiming to explore new chemical pathways and develop innovative products.

In Indonesian laboratories, 2-Bromobenzaldehyde is frequently used in organic chemistry research, supporting both academic and industrial initiatives. It is a staple in chemical synthesis processes, aiding in the development of pharmaceuticals, cosmetics, and other specialty chemicals. Its availability in various packaging sizes ensures that it is suitable for both small-scale experiments and larger research projects, making it an essential component in the chemical toolkit of Indonesian scientists.

Related TCI products

Synthesis of complex aromatic compounds due to its reactivity and functional group versatility.
Nucleophilic substitution reactions where it acts as a good electrophilic substrate.
Coupling reactions for the formation of heterocyclic structures in medicinal chemistry.
Development of pharmaceutical intermediates through functional group modification.
Research in cosmetic chemistry for the creation of fragrance and active ingredient compounds.

Brand	TCI
CAS number	6630-33-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various sizes to suit different laboratory needs
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

2-Bromobenzaldehyde should be stored in a cool, dry place, away from direct light and incompatible substances such as strong oxidizers. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation and to avoid contact with skin or inhalation. Always follow standard chemical safety protocols to minimize risks during handling and storage.

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