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TCI

CAS 612-23-7

2-Nitrobenzyl Chloride TCI N0182

2-Nitrobenzyl Chloride TCI N0182

Chemical Identity

CAS No.
612-23-7
PubChem
CID 11921·SID 87573559
Formula
C7H6ClNO2
Molecular weight
171.58 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-(chloromethyl)-2-nitrobenzene
SMILES
C1=CC=C(C(=C1)CCl)[N+](=O)[O-]
InChIKey
BXCBUWKTXLWPSB-UHFFFAOYSA-N
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2-Nitrobenzyl Chloride is a chemical compound widely used as a building block in various organic reactions. It plays a crucial role in the synthesis of complex organic molecules, particularly in nucleophilic substitution reactions and the formation of new chemical bonds. This compound is a key component in the development of both heterocyclic and non-heterocyclic compounds, making it an essential tool for organic chemists. Its strategic importance lies in its ability to facilitate precise and controlled chemical transformations in laboratory settings.

The compound is valued for its stable chemical structure and predictable reactivity, which make it a preferred choice for synthetic chemists. It dissolves well in organic solvents such as ethyl acetate and chloroform, simplifying purification and reaction processes. These solubility properties enhance its versatility in high-precision applications. Its reliability and consistency contribute to its widespread use in both academic and industrial research environments.

In Indonesian laboratories, 2-Nitrobenzyl Chloride is commonly used in organic chemistry research, especially in the development of new compounds for the pharmaceutical and chemical industries. It is also applied in studies focused on aromatic reactivity and the creation of efficient, environmentally friendly synthesis methods. Its role in advancing chemical innovation is significant, supporting both fundamental research and applied development.

  • Organic synthesis of heterocyclic and non-heterocyclic compounds due to its reactivity and structural versatility.
  • Nucleophilic substitution reactions where it serves as a versatile electrophilic substrate for functional group transformations.
  • Development of pharmaceutical compounds through its use in the synthesis of complex organic molecules with high specificity.
  • Environmental chemistry research for the creation of efficient and sustainable synthetic methodologies.
  • Aromatic reactivity studies to understand substitution patterns and reaction mechanisms in aromatic systems.

Brand TCI
CAS number 612-23-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities as per supplier offerings
Physical form Liquid
Storage Store in a cool, dry place away from light and incompatible materials

2-Nitrobenzyl Chloride should be stored in a cool, dry place, away from direct light and incompatible substances such as strong bases or reducing agents. It is recommended to use sealed containers made of materials compatible with organic solvents, such as glass or high-density polyethylene. In laboratory settings, proper ventilation is essential to minimize exposure to vapors. Always handle the compound with appropriate personal protective equipment, including gloves and safety goggles. Regular monitoring of storage conditions ensures the stability and safety of the material during long-term use.

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