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TCI

CAS 2909-38-8

3-Chlorophenyl Isocyanate TCI I0119

3-Chlorophenyl Isocyanate TCI I0119

Chemical Identity

CAS No.
2909-38-8
PubChem
CID 17968·SID 87571515
Formula
C7H4ClNO
Molecular weight
153.56 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-chloro-3-isocyanatobenzene
SMILES
C1=CC(=CC(=C1)Cl)N=C=O
InChIKey
HHIRBXHEYVDUAM-UHFFFAOYSA-N
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3-Chlorophenyl Isocyanate is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. It serves as a key building block in organic chemistry, particularly in reactions that require high reactivity or electronic activation. This compound is commonly employed in the development of heterocyclic compounds and other organic substances due to its unique molecular structure. Its reactivity makes it a valuable tool for chemists seeking to create new compounds with specific functional groups.

The compound's molecular structure consists of a chloro group attached to a phenyl ring, with an isocyanate group that is highly reactive. These characteristics make it ideal for substitution reactions and the formation of new chemical bonds. The presence of both the chloro and isocyanate functionalities allows for versatile synthetic pathways. Its reactivity and structural versatility are key factors in its widespread use across various chemical applications.

In Indonesian laboratories, 3-Chlorophenyl Isocyanate is a critical reagent for organic synthesis, especially in pharmaceutical and industrial research. It is frequently used in the development of new compounds with potential applications in medicine and chemical industries. Researchers in Indonesia rely on this compound to explore novel synthetic methods and to create compounds with desired properties. Its role in advancing chemical research in the region is significant.

  • Synthesis of heterocyclic compounds for pharmaceutical development due to its reactivity and functional group versatility.
  • Modification of aromatic rings through substitution reactions, leveraging the chloro and isocyanate functionalities.
  • Development of new organic compounds with specific structural features required for industrial applications.
  • Research in medicinal chemistry to create compounds with potential therapeutic properties.
  • Exploration of novel synthetic pathways in organic chemistry for advanced chemical innovation.

Brand TCI
CAS number 2909-38-8
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 moisture and direct sunlight

3-Chlorophenyl Isocyanate should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area with appropriate personal protective equipment. Avoid contact with skin and eyes, and ensure proper disposal procedures are followed. The compound requires careful handling to prevent accidental reactions or contamination. Storage conditions should be controlled to ensure safety and effectiveness in laboratory use.

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