2-Bromo-N,N-dimethylaniline TCI B3243

Chemical Identity

CAS No.: 698-00-0
PubChem: CID 136527·SID 87560738
Formula: C8H10BrN
Molecular weight: 200.08 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromo-N,N-dimethylaniline
SMILES: CN(C)C1=CC=CC=C1Br
InChIKey: ONMSBNJJCUCYED-UHFFFAOYSA-N

Rp 928.200,00

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2-Bromo-N,N-dimethylaniline is a chemical compound widely used in organic synthesis reactions within laboratory settings. As a building block in the field of chemistry, it serves as a versatile reagent for creating complex molecular structures. Its unique structure, featuring a bromo group attached to an N,N-dimethylaniline moiety, makes it a valuable component in the development of various chemical compounds. This compound is particularly useful in reactions that require substitution or nucleophilic mechanisms, making it a key player in synthetic chemistry.

The chemical properties of 2-Bromo-N,N-dimethylaniline, including its basic nature and reactivity, make it a preferred choice for many synthetic applications. It can participate in a range of reactions such as SN1, SN2, and condensation reactions, which are essential in the synthesis of heterocyclic compounds and bioactive molecules. Its ability to react with acids and its molecular complexity further enhance its utility in laboratory research. These characteristics position it as a fundamental reagent in the synthesis of pharmaceuticals and other specialized chemical products.

In Indonesian laboratories, 2-Bromo-N,N-dimethylaniline is commonly used in organic chemistry research, especially in the development of pharmaceutical compounds and specialty chemicals. Its role in creating complex molecular structures makes it an essential material for chemists working on drug synthesis and other advanced chemical applications. The compound's reactivity and structural versatility ensure its continued use in both academic and industrial research settings.

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactivity and structural versatility.
Preparation of bioactive molecules as a key intermediate in pharmaceutical research.
Conducting nucleophilic substitution reactions because of its bromo group and amine functionality.
Development of specialty chemicals through its participation in condensation and SN1/SN2 reactions.
Research in medicinal chemistry for the synthesis of drug-related compounds and derivatives.

Brand	TCI
CAS number	698-00-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

2-Bromo-N,N-dimethylaniline should be stored in a cool, dry place away from direct light and incompatible substances. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene. Due to its reactivity and basic nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound. Avoid contact with acids and strong oxidizing agents to prevent unwanted reactions. Always follow standard laboratory safety protocols to ensure safe handling and storage.

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