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CAS 35450-37-4

Methyl 3-Bromo-4-methoxybenzoate TCI M2264

Methyl 3-Bromo-4-methoxybenzoate TCI M2264

Chemical Identity

CAS No.
35450-37-4
PubChem
CID 611662·SID 135727084
Formula
C9H9BrO3
Molecular weight
245.07 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 3-bromo-4-methoxybenzoate
SMILES
COC1=C(C=C(C=C1)C(=O)OC)Br
InChIKey
ZREVPFANJBZHEU-UHFFFAOYSA-N
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Methyl 3-Bromo-4-methoxybenzoate is a chemical compound widely used as a building block in organic synthesis. It plays a crucial role in laboratory settings where researchers aim to create complex molecules through various chemical reactions. This compound is particularly valuable in pharmaceutical and organic chemistry applications due to its versatility and reactivity. Its presence in synthetic pathways allows for the development of new compounds with tailored properties, making it a key component in advanced chemical research.

The compound's stability and controlled reactivity make it a preferred choice for chemists working on intricate molecular structures. The bromo and methoxy groups on its molecular structure contribute to its unique reactivity, enabling participation in nucleophilic substitution and Friedel-Crafts reactions. These properties ensure that it remains a reliable and effective reagent in both academic and industrial chemical processes. Its ability to undergo various chemical transformations also makes it a versatile tool in the synthesis of pharmaceuticals and other organic compounds.

In Indonesian laboratories, Methyl 3-Bromo-4-methoxybenzoate is commonly used in pure and applied chemical research. It is particularly relevant in the development of new drugs and industrial chemicals, where high-quality starting materials are essential. Its availability and reliability make it a preferred choice for local researchers seeking to conduct advanced chemical experiments with consistent results.

  • Drug synthesis applications benefit from this compound's ability to undergo bromo substitution, enabling the creation of complex pharmaceutical molecules.
  • Organic chemistry research relies on its reactivity in esterification reactions, supporting the development of new chemical structures.
  • Industrial chemical development utilizes its stability and controlled reactivity for the production of specialized compounds.
  • Academic research projects use it as a key reagent in the exploration of molecular transformations and reaction mechanisms.
  • Analytical chemistry experiments incorporate it as a reference standard for testing and validating chemical processes.

Brand TCI
CAS number 35450-37-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light

Methyl 3-Bromo-4-methoxybenzoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be handled in a well-ventilated area to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. It is important to avoid direct contact with skin and eyes, and to follow standard chemical safety protocols. Proper storage and handling ensure the compound remains effective and safe for use in laboratory applications.

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