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Catalog Number:
19201
CAS Number:
66670-54-0
Ester éthylique de l'acide 6-chloro-2 H -chromène-3-carboxylique
Purity:
≥ 94 % (HPLC)
Synonym(s):
6-chloro-2 H -chromène-3-carboxylate d'éthyle
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$132.20 /100 mg
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Product Information

6-Chloro-2H-chromene-3-carboxylic acid ethyl ester is a versatile compound recognized for its significant applications in organic synthesis and medicinal chemistry. This compound, also known as ethyl 6-chloro-2H-chromene-3-carboxylate, features a unique chromene structure that enhances its reactivity and functional properties. Its ability to act as a building block in the synthesis of various bioactive molecules makes it invaluable in the development of pharmaceuticals and agrochemicals. Researchers have utilized this compound in the synthesis of novel compounds with potential anti-inflammatory and anticancer activities, showcasing its relevance in drug discovery.

Moreover, the compound's stability and ease of modification allow for the creation of derivatives tailored for specific applications, making it a preferred choice for chemists looking to innovate in their projects. Its unique properties enable it to serve as a key intermediate in the production of dyes and pigments, further expanding its utility across different industries. With its promising applications and benefits, 6-Chloro-2H-chromene-3-carboxylic acid ethyl ester stands out as a valuable asset for researchers and industry professionals alike.

Synonyms
6-chloro-2 H -chromène-3-carboxylate d'éthyle
CAS Number
66670-54-0
Purity
≥ 94 % (HPLC)
Molecular Formula
C12H11ClO3
Molecular Weight
238.67
MDL Number
MFCD00244132
PubChem ID
1475944
Melting Point
113-119 ?C
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
6-chloro-2 H -chromène-3-carboxylate d'éthyle
CAS Number
66670-54-0
Purity
≥ 94 % (HPLC)
Molecular Formula
C12H11ClO3
Molecular Weight
238.67
MDL Number
MFCD00244132
PubChem ID
1475944
Melting Point
113-119 ?C
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-Chloro-2H-chromene-3-carboxylic acid ethyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Organic Synthesis: It is commonly used in organic chemistry for the construction of complex molecules, making it valuable for researchers developing new chemical entities.
  • Material Science: The compound is explored for its potential in creating novel materials, such as polymers and coatings, which can offer improved durability and chemical resistance.
  • Biological Research: It has applications in studying biological pathways due to its ability to interact with specific enzymes, aiding in the understanding of metabolic processes.
  • Natural Product Synthesis: This chemical is employed in the synthesis of natural product analogs, which can lead to the discovery of new bioactive compounds with therapeutic potential.

Citations