2-Benzyl-4-chlorophenol TCI B0812

Chemical Identity

CAS No.: 120-32-1
PubChem: CID 8425·SID 87563799
Formula: C13H11ClO
Molecular weight: 218.68 g/mol
Purity: >97.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-benzyl-4-chlorophenol
SMILES: C1=CC=C(C=C1)CC2=C(C=CC(=C2)Cl)O
InChIKey: NCKMMSIFQUPKCK-UHFFFAOYSA-N

Rp 980.700,00

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2-Benzyl-4-chlorophenol is a chemical compound widely used in laboratory settings for its versatile reactivity and structural characteristics. As a building block in organic chemistry, it plays a crucial role in the synthesis of complex organic molecules. Its aromatic structure, combined with substituents such as chlorine and benzyl groups, makes it a valuable intermediate in various chemical reactions. This compound is commonly found in research environments where the development of new chemical compounds and materials is the primary goal. Its ability to participate in electrophilic reactions and substitution processes makes it a preferred choice for chemists working on diverse synthetic pathways.

The compound's reactivity is further enhanced by its solubility in common organic solvents such as ethyl acetate and chloroform. These properties allow it to be easily incorporated into reaction mixtures, facilitating efficient chemical transformations. Additionally, its stability under certain conditions ensures that it remains effective throughout the duration of experiments. This stability, coupled with its reactivity, makes it a reliable and consistent material for laboratory use. Its ability to undergo substitution and oxidation reactions also broadens its applicability in both academic and industrial research settings.

In Indonesian laboratories, 2-Benzyl-4-chlorophenol is frequently used in organic chemistry research, particularly in educational institutions and research organizations. It is a common choice for students and researchers due to its well-defined chemical properties and predictable behavior in various reaction conditions. Its role in the synthesis of more complex molecules makes it an essential tool for those engaged in chemical research and development.

Related TCI products

Organic synthesis is a primary application where 2-Benzyl-4-chlorophenol is used for its reactivity in substitution and oxidation reactions.
It is suitable for electrophilic substitution reactions due to its aromatic structure and substituents, making it ideal for Friedel-Crafts reactions.
The compound is commonly used in the development of new chemical compounds, especially in research focused on molecular synthesis and functional group transformations.
It is a preferred material in academic laboratories for teaching and research in organic chemistry, offering hands-on experience with reactive intermediates.
Its solubility in organic solvents makes it suitable for use in a wide range of experimental setups, including solution-based reactions and chromatographic techniques.

Brand	TCI
CAS number	120-32-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid, typically in crystalline or powder form
Storage	Store in a cool, dry place away from light and incompatible materials

2-Benzyl-4-chlorophenol should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be stored separately from strong oxidizing agents and incompatible substances. Proper ventilation is essential when handling the compound to minimize exposure to vapors. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when working with this material. Regular monitoring of storage conditions ensures the compound remains stable and safe for use in research applications.

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