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Catalog Number:
42622
CAS Number:
1820711-54-3
6-(1-naphtylamino)-1,4-benzodioxane
Purity:
≥ 97% (CG)
Synonym(s):
N- [2,3-Dihydrobenzo[1,4]dioxin-6-yl]-1-naphtylamine
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Product Information

6-(1-Naphthylamino)-1,4-benzodioxane is a versatile compound known for its unique structural properties, making it a valuable asset in various research and industrial applications. This compound features a naphthylamine moiety, which enhances its potential as a building block in organic synthesis and medicinal chemistry. Its distinctive benzodioxane structure allows for intriguing interactions in biological systems, positioning it as a candidate for drug development and therapeutic research.

Researchers have explored the use of 6-(1-Naphthylamino)-1,4-benzodioxane in the synthesis of novel pharmaceuticals, particularly in the development of compounds targeting specific biological pathways. Its ability to act as a ligand in coordination chemistry also opens avenues for applications in catalysis and material science. With its promising properties and potential for innovation, this compound stands out as a key ingredient for professionals seeking to advance their projects in chemical synthesis and drug discovery.

Synonyms
N- [2,3-Dihydrobenzo[1,4]dioxin-6-yl]-1-naphtylamine
CAS Number
1820711-54-3
Purity
≥ 97% (CG)
Molecular Formula
C 18 H 15 NON 2
Molecular Weight
277.32
MDL Number
MFCD11975435
PubChem ID
44629971
Melting Point
133 - 137 °C
Appearance
Poudre cristalline jaune clair à jaune à orange
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
N- [2,3-Dihydrobenzo[1,4]dioxin-6-yl]-1-naphtylamine
CAS Number
1820711-54-3
Purity
≥ 97% (CG)
Molecular Formula
C 18 H 15 NON 2
Molecular Weight
277.32
MDL Number
MFCD11975435
PubChem ID
44629971
Melting Point
133 - 137 °C
Appearance
Poudre cristalline jaune clair à jaune à orange
Conditions
Conserver entre 2 et 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-(1-Naphthylamino)-1,4-benzodioxane is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is explored for its potential as a therapeutic agent in treating various diseases, particularly in the field of oncology, where its unique structure may enhance drug efficacy.
  • Biochemical Research: It serves as a valuable tool in studying enzyme interactions and cellular processes, helping researchers understand complex biological mechanisms.
  • Material Science: The compound is investigated for its properties in developing advanced materials, such as polymers and coatings, which can offer improved durability and performance.
  • Analytical Chemistry: It is used as a reference standard in chromatography and spectrometry, assisting in the accurate identification and quantification of similar compounds in various samples.
  • Environmental Studies: Researchers are examining its behavior in environmental systems, contributing to the understanding of chemical fate and transport in ecosystems.

Citations