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CAS 2243-83-6

2-Naphthoyl Chloride TCI N0048

2-Naphthoyl Chloride TCI N0048

Chemical Identity

CAS No.
2243-83-6
PubChem
CID 75246·SID 87573456
Formula
C11H7ClO
Molecular weight
190.62 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
naphthalene-2-carbonyl chloride
SMILES
C1=CC=C2C=C(C=CC2=C1)C(=O)Cl
InChIKey
XNLBCXGRQWUJLU-UHFFFAOYSA-N
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2-Naphthoyl Chloride is a chemical compound widely used in various chemical reactions for the synthesis of complex molecules. It serves as a fundamental building block in organic chemistry, particularly in the creation of aromatic compounds and their derivatives. This compound is commonly found in chemical laboratories as a key reagent that can react with different functional groups to form new compounds. Its role is essential in the development of synthetic pathways that require precise chemical transformations.

The compound is valued for its stable yet reactive nature, making it a preferred choice in laboratory settings. Its molecular structure is well-defined, ensuring consistent chemical behavior during experiments. Additionally, its solubility in organic solvents makes it ideal for reactions that do not involve aqueous media. This solubility characteristic enhances its versatility in different synthetic approaches. The chemical stability of 2-Naphthoyl Chloride also minimizes the risk of degradation during storage and use, ensuring reliable performance in laboratory applications.

In Indonesian laboratories, 2-Naphthoyl Chloride is frequently used in organic chemistry research, especially in the synthesis of aromatic compounds and their derivatives. Its availability and high quality make it a popular choice among research institutions and educational facilities. The compound supports a wide range of chemical investigations, contributing to the advancement of scientific knowledge in the field of organic chemistry.

  • Organic synthesis of aromatic compounds due to its reactivity and structural versatility.
  • Preparation of derivatives through functional group transformations in chemical reactions.
  • Research in medicinal chemistry for the development of pharmaceutical compounds.
  • Teaching and experimental use in undergraduate and graduate chemistry courses.
  • Development of new materials through chemical modification of aromatic structures.

Brand TCI
CAS number 2243-83-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply.
Physical form Solid or liquid, depending on the specific product variant.
Storage Store in a cool, dry place away from moisture and direct sunlight.

2-Naphthoyl Chloride should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and exposure to air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to ensure safety. Avoid contact with incompatible substances such as strong bases or reducing agents. Always wear appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper storage and handling practices help minimize risks and ensure the compound remains effective for laboratory use.

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