4-Bromo-2-methylbenzyl Alcohol TCI B5231

Chemical Identity

CAS No.: 17100-58-2
PubChem: CID 22280088·SID 354334378
Formula: C8H9BrO
Molecular weight: 201.06 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (4-bromo-2-methylphenyl)methanol
SMILES: CC1=C(C=CC(=C1)Br)CO
InChIKey: IFKWLKCPUIQXPU-UHFFFAOYSA-N

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4-Bromo-2-methylbenzyl Alcohol is a chemical compound widely used as a building block in organic synthesis. It serves as a key intermediate in the development of complex organic molecules, particularly in reactions involving bromo substitution and heterocyclic ring formation. Its structural simplicity allows for versatile chemical transformations, making it a valuable resource for chemists working in both academic and industrial settings. This compound is essential for researchers aiming to design and synthesize new pharmaceuticals, agrochemicals, and specialty chemicals.

The compound's chemical properties make it a preferred choice for various laboratory applications. It exhibits high polarity due to the presence of both hydroxyl and bromo groups, enabling solubility in organic solvents such as ethyl acetate and ethanol. This solubility profile supports its use in reactions requiring high reactivity and stability under controlled conditions. Additionally, its stability in certain environments enhances its reliability as a reagent in synthetic processes. However, it remains sensitive to heat and UV light, necessitating careful handling and storage.

In Indonesian laboratories, 4-Bromo-2-methylbenzyl Alcohol is commonly used in organic chemistry research, particularly in higher education institutions and research centers. Its availability and adherence to international quality standards make it a trusted material for both teaching and advanced research. The compound's role in synthetic pathways supports its widespread use in the development of new chemical compounds and materials.

Related TCI products

Organic synthesis reactions where bromo substitution and hydroxyl functionality are required.
Heterocyclic compound formation due to its ability to participate in ring-opening and cyclization reactions.
Reactions involving hydrolysis or oxidation where polar functional groups are essential.
Solvent-based reactions that benefit from the compound’s solubility in organic solvents.
Research applications in pharmaceutical and agrochemical development requiring versatile intermediates.

Brand	TCI
CAS number	17100-58-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard chemical supply practices
Physical form	Liquid
Storage	Store in a cool, dark place away from heat and UV light

This compound should be stored in a cool, dark environment to prevent degradation due to heat and UV exposure. It is recommended to keep it in a tightly sealed container made of glass or high-density polyethylene to minimize contamination and evaporation. Due to its polar nature, it is important to handle it with appropriate personal protective equipment, including gloves and safety goggles, to avoid skin contact or inhalation. The compound should be stored away from incompatible materials such as strong oxidizers or acids. Regular monitoring of storage conditions ensures the compound remains chemically stable and suitable for use in laboratory applications.

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