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TCI

CAS 612-13-5

2-Cyanobenzyl Chloride TCI C2656

2-Cyanobenzyl Chloride TCI C2656

Chemical Identity

Other names
2-(Chloromethyl)benzonitrile · alpha-Chloro-o-tolunitrile
CAS No.
612-13-5
PubChem
CID 69152·SID 172088997
Formula
C8H6ClN
Molecular weight
151.59 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(chloromethyl)benzonitrile
SMILES
C1=CC=C(C(=C1)CCl)C#N
InChIKey
ZSHNOXOGXHXLAV-UHFFFAOYSA-N
MDL
MDL00019745
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2-Cyanobenzyl Chloride (TCI C2656) is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It contains both a chloro group and a cyano group, making it a versatile reagent in organic chemistry. This compound is essential in various chemical reactions, particularly in substitution and coupling reactions, where it contributes to the formation of new molecular structures. Its role in laboratory settings is crucial for researchers aiming to develop compounds with specific chemical or biological properties.

The compound is known for its reactivity and chemical stability under controlled conditions. Its ability to participate in a wide range of chemical transformations makes it a preferred choice for synthetic chemists. The presence of both functional groups allows for multiple reaction pathways, enhancing its utility in the design of complex molecules. Its reactivity also means that it requires careful handling to ensure safe and effective use in laboratory environments.

In Indonesian laboratories, 2-Cyanobenzyl Chloride is commonly used in organic chemistry research, especially in the development of pharmaceutical compounds and industrial chemicals. It is also a key reagent in studies involving compounds with antioxidant or anticancer properties, which are important areas of research in both academic and industrial settings. Its use is widespread due to its effectiveness and adaptability in various synthetic strategies.

  • Organic synthesis of pharmaceutical compounds due to its reactivity and functional group versatility.
  • Development of industrial chemicals through efficient coupling and substitution reactions.
  • Research on antioxidant and anticancer compounds due to its ability to form complex molecular structures.
  • Synthesis of heterocyclic compounds by participating in nucleophilic substitution reactions.
  • Preparation of functionalized aromatic derivatives for use in polymer and material science applications.

Brand TCI
CAS number 612-13-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from light and incompatible substances

2-Cyanobenzyl Chloride should be stored in a cool, dry place, away from direct light and incompatible materials such as strong bases or reducing agents. It is recommended to use airtight containers made of materials resistant to chemical attack, such as glass or high-density polyethylene. Due to its reactivity and potential toxicity, it should be handled in a well-ventilated area with appropriate personal protective equipment. Avoid exposure to high temperatures and moisture to maintain stability. Always follow standard laboratory safety protocols when working with this compound to ensure safe handling and prevent accidental reactions.

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