2-Bromo-4-chlorophenol TCI B1522

Chemical Identity

CAS No.: 695-96-5
PubChem: CID 69670·SID 87564430
Formula: C6H4BrClO
Molecular weight: 207.45 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromo-4-chlorophenol
SMILES: C1=CC(=C(C=C1Cl)Br)O
InChIKey: ZIYRDJLAJYTELF-UHFFFAOYSA-N

Rp 1.298.850,00

~~Rp 908.250,00~~ Rp 1.298.850,00

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2-Bromo-4-chlorophenol is a chemical compound widely used in laboratory settings for various synthetic reactions, especially in the synthesis of complex organic compounds. This compound belongs to the category of non-heterocyclic building blocks and serves as a versatile reagent in organic chemistry. Its aromatic structure, combined with bromo and chloro substituents, provides unique reactivity, making it a valuable component in chemical synthesis. Due to its stability and reactivity, it is often employed in substitution and oxidation reactions to produce more complex molecular structures.

The compound's chemical properties, including its solubility in organic solvents like ethyl acetate and ethanol, make it convenient for laboratory manipulation. Its consistent performance and reliability are highly appreciated by researchers. The reactivity and structural versatility of 2-Bromo-4-chlorophenol make it a preferred choice for synthetic chemists. Its predictable behavior under various reaction conditions ensures reproducibility and accuracy in experimental outcomes.

In Indonesian laboratories, 2-Bromo-4-chlorophenol is commonly used in organic chemistry research and the synthesis of new compounds. Its availability and cost-effectiveness make it a popular choice for researchers seeking an effective and accessible building block. The compound's role in creating complex molecular structures supports ongoing advancements in chemical research and development within the scientific community.

Related TCI products

Organic synthesis of complex compounds due to its reactivity and structural versatility.
Substitution reactions where bromo and chloro groups can be replaced with other functional groups.
Oxidation processes to modify aromatic rings and create more complex molecular structures.
Research in chemical engineering for developing new materials and pharmaceutical intermediates.
Educational purposes in teaching organic chemistry and synthetic reaction mechanisms.

Brand	TCI
CAS number	695-96-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid or liquid depending on the specific product variant
Storage	Store in a cool, dry place away from direct sunlight and incompatible materials

2-Bromo-4-chlorophenol should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. The compound should be kept away from incompatible substances such as strong oxidizers and acids to avoid chemical reactions. Proper ventilation is essential when handling the material to minimize exposure. Always use appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions helps maintain the compound's stability and effectiveness for laboratory use.

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