3-Bromo-2-methoxybenzoic Acid TCI B5262

Chemical Identity

CAS No.: 101084-39-3
PubChem: CID 253598·SID 468590566
Formula: C8H7BrO3
Molecular weight: 231.04 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromo-2-methoxybenzoic acid
SMILES: COC1=C(C=CC=C1Br)C(=O)O
InChIKey: PIBPHOFXQUUPTM-UHFFFAOYSA-N

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3-Bromo-2-methoxybenzoic Acid is a versatile organic compound widely used in laboratory settings for its reactivity and structural versatility. As a building block in organic synthesis, it serves as a key intermediate in the development of complex molecules. Its aromatic structure, combined with bromo and methoxy substituents, makes it a valuable tool for chemists seeking to modify molecular frameworks. This compound is commonly found in research laboratories, where it supports the synthesis of pharmaceuticals, agrochemicals, and industrial chemicals. Its role in facilitating chemical transformations underscores its importance in both academic and industrial research.

The chemical properties of 3-Bromo-2-methoxybenzoic Acid make it a preferred choice for synthetic chemists. The presence of bromo and methoxy groups enhances its reactivity and polarity, enabling it to participate in various reaction mechanisms such as nucleophilic substitution and electrophilic aromatic substitution. The bromo group contributes to the molecule’s electrophilicity, while the methoxy group increases its polarity, making it suitable for a wide range of synthetic pathways. These characteristics allow it to be used in esterification, coupling reactions, and other functional group transformations, making it a reliable reagent in organic chemistry.

In Indonesian laboratories, 3-Bromo-2-methoxybenzoic Acid is frequently used in scientific research and educational settings. It is a staple in academic institutions and research centers, supporting the development of new compounds and the teaching of organic chemistry principles. Its stability and ease of modification make it an essential component in both basic and advanced chemical studies. As a result, it plays a crucial role in advancing scientific knowledge and innovation in the region.

Related TCI products

Organic synthesis for the preparation of pharmaceuticals and agrochemicals due to its reactivity and structural versatility.
Development of complex molecules through nucleophilic substitution and electrophilic aromatic substitution reactions.
Esterification processes where the methoxy group enhances reactivity and polarity for efficient chemical transformations.
Coupling reactions in the synthesis of diverse organic compounds, leveraging its functional group compatibility.
Educational use in teaching organic chemistry principles, demonstrating key synthetic strategies and molecular modifications.

Brand	TCI
CAS number	101084-39-3
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, crystalline appearance
Storage	Store in a cool, dry place away from direct sunlight and moisture

3-Bromo-2-methoxybenzoic Acid should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances such as strong bases or oxidizing agents. The compound is stable under normal storage conditions but should be protected from light and heat to ensure long-term usability. Proper storage ensures the compound remains effective for its intended applications in laboratory research.

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