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CAS 14804-38-7

4-Bromo-2,6-dimethylanisole TCI B3016

4-Bromo-2,6-dimethylanisole TCI B3016

Chemical Identity

CAS No.
14804-38-7
PubChem
CID 278654·SID 87559411
Formula
C9H11BrO
Molecular weight
215.09 g/mol
Purity
>96.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
5-bromo-2-methoxy-1,3-dimethylbenzene
SMILES
CC1=CC(=CC(=C1OC)C)Br
InChIKey
MMARFGDTMJBIBK-UHFFFAOYSA-N
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4-Bromo-2,6-dimethylanisole is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a versatile building block for creating more complex molecular structures, particularly in the development of aromatic compounds. This compound is commonly employed in various synthetic pathways where electrophilic substitution reactions are required. Its presence in laboratory workflows highlights its importance in advancing chemical research and innovation.

The compound's chemical structure, featuring a bromo group at position 4 and methyl groups at positions 2 and 6, contributes to its reactivity and utility. The bromo group imparts strong electrophilic properties, making it ideal for substitution reactions. The methyl groups enhance the molecule’s stability and influence its overall reactivity. These characteristics make it a preferred choice for chemists seeking reliable and effective reagents.

In Indonesian laboratories, 4-Bromo-2,6-dimethylanisole is extensively used in organic chemistry research, especially in the synthesis of aromatic compounds and their derivatives. Its stability under normal conditions simplifies storage and handling, making it a valuable resource for both academic and industrial research. The compound’s role in building complex structures underscores its significance in chemical experimentation and development.

  • Organic synthesis reactions benefit from this compound’s electrophilic nature, enabling efficient substitution processes in aromatic ring systems.
  • It is ideal for Friedel-Crafts reactions due to its ability to participate in electrophilic aromatic substitution, enhancing reaction yields.
  • Nitration processes can be optimized using this compound as a starting material, providing a stable and reactive intermediate.
  • It supports the development of aromatic derivatives, offering a reliable foundation for creating complex molecular architectures.
  • Its stability and reactivity make it suitable for structural modification studies, aiding in the design of new chemical compounds.

Brand TCI
CAS number 14804-38-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities as per supplier specifications
Physical form Solid crystalline powder
Storage Store in a cool, dry place away from direct light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its electrophilic nature, it should be handled with care in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to incompatible substances such as strong oxidizers. Proper labeling and storage conditions ensure safe handling and long-term usability in laboratory applications.

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