Methyl 3-(Bromomethyl)benzoate TCI B2224

Chemical Identity

CAS No.: 1129-28-8
PubChem: CID 517981·SID 87565078
Formula: C9H9BrO2
Molecular weight: 229.07 g/mol
Purity: >97.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3-(bromomethyl)benzoate
SMILES: COC(=O)C1=CC=CC(=C1)CBr
InChIKey: YUHSMQQNPRLEEJ-UHFFFAOYSA-N

Rp 1.908.900,00

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Berat 5g 25g

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Methyl 3-(Bromomethyl)benzoate is a chemical compound widely utilized in organic synthesis reactions within laboratory settings. This compound serves as a key building block in the development of more complex molecules, making it essential for researchers in both academic and industrial environments. Its unique molecular structure enables it to participate in various synthetic pathways, particularly in substitution and cross-coupling reactions. Due to its reactivity and versatility, it is a valuable tool for chemists aiming to create new compounds with specific functional groups or biological activities.

The compound’s bromomethyl group contributes to its high reactivity, making it ideal for reactions that require electrophilic activation or nucleophilic substitution. Its chemical stability under controlled laboratory conditions ensures consistent performance in synthetic processes. Additionally, its molecular structure allows for the synthesis of heterocyclic compounds and bioactive molecules, expanding its applications in pharmaceutical and chemical research. These properties make it a preferred choice for laboratories seeking reliable and effective reagents.

In Indonesian laboratories, Methyl 3-(Bromomethyl)benzoate is commonly used in organic chemistry research, particularly in academic institutions and research centers. It plays a crucial role in the development of new compounds with potential applications in medicine and industry. Its availability through suppliers like AMI Scientific ensures that researchers have access to this essential reagent for their experimental needs.

Related TCI products

Organic synthesis reactions where bromomethyl groups are needed for functional group modification.
Cross-coupling reactions that require electrophilic activation and high reactivity.
Development of heterocyclic compounds with specific biological or pharmaceutical properties.
Research into bioactive molecules that require precise structural modifications.
Synthesis of complex organic compounds for industrial and academic applications.

Brand	TCI
CAS number	1129-28-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid depending on the specific formulation
Storage	Store in a cool, dry place away from light and moisture

Methyl 3-(Bromomethyl)benzoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactive nature, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid contact with incompatible materials such as strong bases or reducing agents. Proper labeling and storage conditions are essential to ensure safety and maintain the integrity of the compound during laboratory use.

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