3-Cyanophenacyl Bromide TCI B4079

Chemical Identity

CAS No.: 50916-55-7
PubChem: CID 2735867·SID 253659723
Formula: C9H6BrNO
Molecular weight: 224.05 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-(2-bromoacetyl)benzonitrile
SMILES: C1=CC(=CC(=C1)C(=O)CBr)C#N
InChIKey: XWCGNFLHRINYCE-UHFFFAOYSA-N

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3-Cyanophenacyl Bromide (TCI B4079) is a chemical compound widely used in organic synthesis as a key building block in the laboratory. This compound plays a crucial role in the development of complex organic molecules, particularly in reactions involving substitution and bond formation. Its unique molecular structure, containing both a bromide and a cyanide group, makes it highly versatile for various chemical transformations. Due to its reactivity and functional group versatility, it is a valuable tool for chemists working on synthetic pathways.

The compound is known for its solubility in organic solvents such as ethyl acetate and ethanol, which facilitates its use in a wide range of experimental conditions. Its stability under specific reaction conditions further enhances its utility in laboratory settings. Additionally, its ability to participate in both nucleophilic and electrophilic reactions makes it a preferred choice for synthetic chemists. These properties allow it to be used in both academic and industrial research environments.

In Indonesian laboratories, 3-Cyanophenacyl Bromide is commonly used in organic chemistry research, particularly in higher education institutions and research centers. It is an essential component in the synthesis of new compounds with applications in pharmaceuticals and chemical materials. Its role in the development of heterocyclic and non-heterocyclic compounds makes it a staple in chemical laboratories across Indonesia.

Related TCI products

Organic synthesis of heterocyclic and non-heterocyclic compounds due to its reactive functional groups and structural versatility.
Preparation of pharmaceutical intermediates through nucleophilic and electrophilic substitution reactions.
Development of new chemical materials by facilitating bond formation and molecular modification.
Research in medicinal chemistry for the synthesis of bioactive compounds with therapeutic potential.
Educational use in undergraduate and graduate chemistry courses for teaching synthetic methodologies.

Brand	TCI
CAS number	50916-55-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light and moisture

3-Cyanophenacyl Bromide should be stored in a cool, dry place, away from light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care in a well-ventilated laboratory environment. Avoid exposure to incompatible substances such as strong bases or reducing agents. Proper personal protective equipment, including gloves and safety goggles, should always be worn when handling this compound. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.

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