Methyl 3,5-Dibromo-4-methylbenzoate TCI D2871

Chemical Identity

Other names: 3,5-Dibromo-p-toluic Acid Methyl Ester · 3,5-Dibromo-4-methylbenzoic Acid Methyl Ester · Methyl 3,5-Dibromo-p-toluate
CAS No.: 74896-66-5
PubChem: CID 624016·SID 87569249
Formula: C9H8Br2O2
Molecular weight: 307.97 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3,5-dibromo-4-methylbenzoate
SMILES: CC1=C(C=C(C=C1Br)C(=O)OC)Br
InChIKey: SRLAXDDPVYZYNI-UHFFFAOYSA-N
MDL: MDL00010729

Rp 928.200,00

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Methyl 3,5-Dibromo-4-methylbenzoate is a chemical compound widely used in organic synthesis reactions within laboratory settings. This compound serves as a key building block for the creation of complex aromatic structures featuring bromo and methyl substituents. Its role is critical in the development of new chemical compounds and in the study of molecular structures. Due to its stability and controlled reactivity, it is a reliable choice for precise and accurate experimental work.

The compound’s well-defined chemical structure and high consistency make it ideal for identification and application in various chemical reactions. Its non-polar nature allows it to dissolve in organic solvents such as chloroform or ethyl acetate, making it suitable for nucleophilic substitution reactions and the synthesis of complex compounds. These properties contribute to its versatility and effectiveness in laboratory environments.

In Indonesian laboratories, Methyl 3,5-Dibromo-4-methylbenzoate is commonly used in research and development projects focused on organic chemistry. It is a preferred material for students and researchers due to its reliability and ease of handling. Its stability and solubility properties ensure consistent results, supporting both educational and industrial applications.

Related TCI products

Organic synthesis reactions where bromo and methyl substituents are required for structural complexity.
Development of new chemical compounds with aromatic frameworks and functional groups.
Nucleophilic substitution reactions due to its solubility in organic solvents and reactivity.
Research in molecular structure analysis and compound characterization.
Educational experiments in chemistry laboratories for teaching synthesis techniques.

Brand	TCI
CAS number	74896-66-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid crystalline
Storage	Store in a cool, dry place away from light

Methyl 3,5-Dibromo-4-methylbenzoate should be stored in a cool, dry place away from direct light to maintain its stability and prevent degradation. It is recommended to use airtight containers made of glass or polyethylene to protect the compound from moisture and air exposure. Due to its non-polar nature, it is important to handle it with care to avoid contamination. In laboratory settings, it should be kept in a well-ventilated area and stored separately from incompatible substances. Proper labeling and storage conditions ensure the compound remains safe and effective for use in chemical experiments.

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