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Catalog Number:
41808
CAS Number:
63149-33-7
2,3,6,7-Tetrahydro-8-hydroxy-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde
Grade:
suitable for Hematology & Histology
Purity:
≥ 97.5% (GC)
Synonym(s):
9-Formyl-8-hydroxyjulolidine
Documents
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Product Information

2,3,6,7-Tetrahydro-8-hydroxy-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde is a versatile compound recognized for its unique structural features and potential applications in various fields. This compound, often utilized in pharmaceutical research, exhibits properties that make it a valuable candidate for the development of novel therapeutic agents. Its hydroxyl and aldehyde functional groups contribute to its reactivity, allowing for diverse chemical modifications that can enhance biological activity. Researchers have explored its potential in synthesizing compounds with anti-inflammatory and anti-cancer properties, making it a focal point in medicinal chemistry.

In addition to its pharmaceutical relevance, 2,3,6,7-Tetrahydro-8-hydroxy-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde can serve as a building block in organic synthesis, facilitating the creation of complex molecular architectures. Its unique tricyclic structure offers distinct advantages over similar compounds, providing researchers with a robust framework for exploring new chemical entities. This compound's ability to participate in various chemical reactions positions it as a key player in the development of innovative solutions across multiple industries, including agrochemicals and materials science.

Synonyms
9-Formyl-8-hydroxyjulolidine
CAS Number
63149-33-7
Purity
≥ 97.5% (GC)
Grade
suitable for Hematology & Histology
Molecular Formula
C13H15NO2
Molecular Weight
217.26
MDL Number
MFCD00192477
PubChem ID
113099
Melting Point
72 - 74 °C (Lit.)
Appearance
Yellow, tan or green powder or crystals
Conditions
Store at RT
General Information
Synonyms
9-Formyl-8-hydroxyjulolidine
CAS Number
63149-33-7
Purity
≥ 97.5% (GC)
Grade
suitable for Hematology & Histology
Molecular Formula
C13H15NO2
Molecular Weight
217.26
MDL Number
MFCD00192477
PubChem ID
113099
Melting Point
72 - 74 °C (Lit.)
Appearance
Yellow, tan or green powder or crystals
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,3,6,7-Tetrahydro-8-hydroxy-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various bioactive molecules, aiding in the development of new medications.
  • Neuroscience Research: Its unique structure allows for exploration in neuropharmacology, particularly in studying its effects on neurotransmitter systems.
  • Organic Synthesis: It is used as a building block in organic chemistry, facilitating the creation of complex chemical structures in laboratory settings.
  • Material Science: The compound's properties make it suitable for developing advanced materials, such as polymers with specific functional characteristics.
  • Analytical Chemistry: It can be employed as a standard in various analytical techniques, helping researchers ensure the accuracy and reliability of their experimental results.

Citations