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Catalog Number:
28535
CAS Number:
837-32-1
1-Cyclohexyl-5-ethylbarbituric acid
Purity:
≥ 99% (GC)
Documents
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Product Information

1-Cyclohexyl-5-ethylbarbituric acid is a versatile compound known for its applications in pharmaceuticals and research. This barbituric acid derivative exhibits sedative and hypnotic properties, making it valuable in the development of medications aimed at treating anxiety and sleep disorders. Its unique structure allows for enhanced bioavailability and efficacy compared to other barbiturates, which can lead to improved patient outcomes. Researchers appreciate its role in synthesizing various derivatives that can be tailored for specific therapeutic effects, thus expanding its utility in drug formulation.

In addition to its pharmaceutical applications, 1-Cyclohexyl-5-ethylbarbituric acid serves as a key intermediate in organic synthesis, facilitating the production of complex molecules in medicinal chemistry. Its stability and reactivity make it an ideal candidate for various chemical reactions, including condensation and cyclization processes. This compound's potential for innovation in drug development and synthesis positions it as a valuable asset for researchers and industry professionals seeking effective solutions in therapeutic applications.

CAS Number
837-32-1
Purity
≥ 99% (GC)
Molecular Formula
C12H18N2O3
Molecular Weight
238.29
MDL Number
MFCD01665947
PubChem ID
13276
Appearance
Off-white to yellow crystalline powder
Conditions
Store at 0-8 °C
General Information
CAS Number
837-32-1
Purity
≥ 99% (GC)
Molecular Formula
C12H18N2O3
Molecular Weight
238.29
MDL Number
MFCD01665947
PubChem ID
13276
Appearance
Off-white to yellow crystalline powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-Cyclohexyl-5-ethylbarbituric acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a precursor in the synthesis of various barbiturate derivatives, which are important in developing sedatives and anesthetics.
  • Analytical Chemistry: It is used as a standard in chromatographic techniques, aiding researchers in the identification and quantification of similar compounds in complex mixtures.
  • Neuroscience Research: The compound's sedative properties make it valuable in studying the effects of barbiturates on the central nervous system, helping to understand their mechanisms of action.
  • Veterinary Medicine: It finds applications in formulating anesthetics for animal surgeries, providing effective sedation with a favorable safety profile compared to other agents.
  • Organic Synthesis: The unique structure allows for its use in various organic reactions, making it a versatile building block for synthesizing more complex chemical entities.

Citations