4'-Bromomethyl-2-cyanobiphenyl TCI B1806

Chemical Identity

CAS No.: 114772-54-2
PubChem: CID 1501912·SID 87564698
Formula: C14H10BrN
Molecular weight: 272.14 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-[4-(bromomethyl)phenyl]benzonitrile
SMILES: C1=CC=C(C(=C1)C#N)C2=CC=C(C=C2)CBr
InChIKey: LFFIEVAMVPCZNA-UHFFFAOYSA-N

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4'-Bromomethyl-2-cyanobiphenyl is a chemical compound widely used in organic synthesis reactions, particularly in the development of complex molecules with biphenyl structures. This compound serves as a key building block in the synthesis of heterocyclic compounds and other organic substances due to its unique molecular structure. Its core biphenyl framework is modified with a cyanide group and a bromomethyl substituent, making it highly versatile for chemical transformations. In laboratory settings, it plays a crucial role in facilitating nucleophilic substitution and coupling reactions, which are essential for creating more complex molecular architectures.

The compound is valued for its chemical stability under specific reaction conditions and its ability to participate in high-reactivity chemical processes. Its molecular structure allows for easy modification through various chemical reactions, enabling the synthesis of a wide range of new compounds with diverse applications. This adaptability makes it a preferred choice for researchers aiming to develop novel materials or pharmaceuticals. Additionally, its resistance to degradation ensures reliable performance in long-term experiments, making it a trusted reagent in chemical laboratories.

In Indonesian laboratories, 4'-Bromomethyl-2-cyanobiphenyl is commonly used in academic and industrial research settings. It is a key component in the development of new chemical products and is frequently employed in synthetic pathways that require precise molecular manipulation. Its availability and chemical properties make it a valuable resource for both educational and applied research in the field of organic chemistry.

Related TCI products

Organic synthesis reactions benefit from this compound's structural versatility, enabling the creation of complex heterocyclic molecules with high specificity.
Nucleophilic substitution reactions utilize its bromomethyl group as a reactive site, facilitating the formation of new carbon-carbon bonds.
Coupling reactions leverage its biphenyl framework for efficient cross-linking, enhancing the structural diversity of synthesized compounds.
Pharmaceutical research employs it as a building block for the development of novel drug candidates with tailored molecular properties.
Materials science applications take advantage of its chemical stability and reactivity to design advanced polymers and functional materials.

Brand	TCI
CAS number	114772-54-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid (may vary depending on supplier packaging)
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and degradation. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. Avoid exposure to moisture and incompatible substances to maintain its stability and effectiveness. Proper labeling and storage conditions are essential to ensure safe handling and long-term usability in laboratory settings.

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