3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(1R,2R)-2-(dipentylamino)cyclohexyl]amino]-3-cyclobutene-1,2-dione

≥98%,99%e.e.

  • Product Code: 70624
  CAS:    1411983-40-8
Molecular Weight: 561.6 g./mol Molecular Formula: C₂₈H₃₇F₆N₃O₂
EC Number: MDL Number:
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Density: Storage Condition: room temperature, dry
Product Description: This chemical is primarily utilized in the field of organic synthesis, particularly in the development of advanced materials and pharmaceuticals. Its unique structure makes it valuable for creating complex molecules with specific properties. It is often employed in the synthesis of bioactive compounds, where its trifluoromethyl groups and cyclohexylamino moieties contribute to enhanced stability and binding affinity. Additionally, it is used in the preparation of specialized dyes and pigments, leveraging its cyclobutene-1,2-dione core for color stability and durability. Researchers also explore its potential in designing catalysts for asymmetric synthesis, taking advantage of its chiral centers to induce stereoselective reactions. Its application extends to the development of high-performance polymers, where its structural components impart desirable thermal and chemical resistance.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿9,837.00
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3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(1R,2R)-2-(dipentylamino)cyclohexyl]amino]-3-cyclobutene-1,2-dione
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of advanced materials and pharmaceuticals. Its unique structure makes it valuable for creating complex molecules with specific properties. It is often employed in the synthesis of bioactive compounds, where its trifluoromethyl groups and cyclohexylamino moieties contribute to enhanced stability and binding affinity. Additionally, it is used in the preparation of specialized dyes and pigments, leveraging its cyclobutene-1,2-dione core for color stability and durability. Researchers also explore its potential in designing catalysts for asymmetric synthesis, taking advantage of its chiral centers to induce stereoselective reactions. Its application extends to the development of high-performance polymers, where its structural components impart desirable thermal and chemical resistance.
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