2-Bromophenol TCI B0630

Chemical Identity

CAS No.: 95-56-7
PubChem: CID 7244·SID 87563638
Formula: C6H5BrO
Molecular weight: 173.01 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

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

Rp 2.016.000,00

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2-Bromophenol is a chemical compound widely used as a foundational material in various laboratory reactions. It is a key reagent in organic chemistry, particularly in the synthesis of complex organic compounds. Its aromatic structure, combined with a bromo group attached to the phenol ring, makes it a versatile building block for chemical synthesis. This compound is commonly employed in laboratory settings to facilitate reactions such as electrophilic substitution, oxidation, and reduction processes. Its reactivity and structural simplicity make it an essential component in the development of new chemical compounds and materials.

The chemical properties of 2-Bromophenol make it a preferred choice for researchers and chemists. It is highly reactive towards strong bases, alkali metals, and organic solvents, which allows it to participate in a wide range of chemical transformations. Its ability to undergo substitution reactions, especially in the presence of catalysts, enhances its utility in synthetic pathways. The presence of both aromatic and brominated functional groups contributes to its reactivity and versatility, making it suitable for multiple experimental applications. These characteristics are particularly valuable in organic chemistry research and industrial chemical synthesis.

In Indonesian laboratories, 2-Bromophenol is extensively used in both pure and applied chemistry research. It is a common reagent in educational institutions and research centers, supporting experiments related to organic synthesis and chemical reactions. Its role in the development of new compounds and materials makes it a critical component in the chemical research landscape of Indonesia. The compound is frequently used in programs focused on the synthesis of novel organic molecules and functional materials.

Related TCI products

Organic synthesis reactions benefit from 2-Bromophenol due to its reactivity and structural versatility, enabling the formation of complex organic compounds through substitution and oxidation processes.
It is ideal for electrophilic substitution reactions, where its aromatic ring and bromo group provide sites for further chemical modifications and functional group transformations.
In oxidation and reduction studies, 2-Bromophenol serves as a valuable reagent for testing reaction mechanisms and catalyst efficiency in laboratory settings.
It is commonly used in the development of new pharmaceuticals and materials, where its chemical properties support the synthesis of target molecules with specific functional groups.
Indonesian research institutions rely on 2-Bromophenol for experimental work in both academic and industrial chemistry, supporting innovation in chemical synthesis and material science.

Brand	TCI
CAS number	95-56-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-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 incompatible materials

2-Bromophenol should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be stored separately from strong bases, alkali metals, and organic solvents to avoid hazardous reactions. Proper labeling and safe handling procedures are essential to ensure laboratory safety. Always use appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Regular inspection of storage conditions is necessary to maintain its chemical integrity and ensure safe usage in laboratory environments.

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