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Catalog Number:
27799
CAS Number:
95095-71-9
2,3-Diamino-6-(trifluorométhyl)-4(3H)-pyrimidinone
Purity:
≥ 99 % (HPLC)
Synonym(s):
2,3-Diamino-6-(trifluorométhyl)-3,4-dihydropyrimidin-4-one
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Product Information

2,3-Diamino-6-(trifluoromethyl)-4(3H)-pyrimidinone is a versatile compound with significant applications in pharmaceutical research and development. This pyrimidinone derivative is recognized for its unique trifluoromethyl group, which enhances its biological activity and stability. Researchers have utilized this compound in the synthesis of various bioactive molecules, particularly in the development of antiviral and anticancer agents. Its structural features allow for modifications that can lead to improved potency and selectivity in therapeutic applications.

In addition to its pharmaceutical relevance, 2,3-Diamino-6-(trifluoromethyl)-4(3H)-pyrimidinone serves as a valuable intermediate in organic synthesis, enabling the creation of complex chemical entities. Its ability to participate in diverse chemical reactions makes it an essential building block for researchers looking to innovate in drug design and development. The compound's favorable properties, including its solubility and reactivity, position it as a preferred choice for professionals aiming to enhance their research outcomes.

Synonyms
2,3-Diamino-6-(trifluorométhyl)-3,4-dihydropyrimidin-4-one
CAS Number
95095-71-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C5H5F3N4O
Molecular Weight
194.12
MDL Number
MFCD00068010
PubChem ID
1485918
Melting Point
218-226 °C
Appearance
Cristaux jaune pâle
Conditions
Conserver à 0-8°C
General Information
Synonyms
2,3-Diamino-6-(trifluorométhyl)-3,4-dihydropyrimidin-4-one
CAS Number
95095-71-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C5H5F3N4O
Molecular Weight
194.12
MDL Number
MFCD00068010
PubChem ID
1485918
Melting Point
218-226 °C
Appearance
Cristaux jaune pâle
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

2,3-Diamino-6-(trifluoromethyl)-4(3H)-pyrimidinone is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of antiviral and anticancer agents, enhancing therapeutic efficacy.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, providing effective solutions for pest control and crop protection, thus supporting sustainable agriculture practices.
  • Biochemical Research: Researchers employ this compound in studies related to nucleic acid interactions, contributing to advancements in genetic research and molecular biology.
  • Material Science: Its unique properties make it valuable in developing advanced materials, including polymers and coatings, which offer improved durability and resistance to environmental factors.
  • Diagnostic Applications: The compound is explored for use in diagnostic reagents, aiding in the detection of specific biomolecules, which is crucial for medical diagnostics and research.

Citations