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Home  > (2S)-2-amino-3-(4-{2-amino-6-[(1R)-1-[4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl]-2,2,2-trifluoroethoxy]pyrimidin-4-yl}phenyl)propanoic acid

AE11348

1033805-28-5 | (2S)-2-amino-3-(4-{2-amino-6-[(1R)-1-[4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl]-2,2,2-trifluoroethoxy]pyrimidin-4-yl}phenyl)propanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
5mg 95% in stock $111.00 $78.00 -   +
10mg 95% in stock $166.00 $117.00 -   +
250mg 95% in stock $837.00 $586.00 -   +
1g 95% in stock $2,097.00 $1,468.00 -   +
5g 95% in stock $6,247.00 $4,373.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE11348
Chemical Name: (2S)-2-amino-3-(4-{2-amino-6-[(1R)-1-[4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl]-2,2,2-trifluoroethoxy]pyrimidin-4-yl}phenyl)propanoic acid
CAS Number: 1033805-28-5
Molecular Formula: C25H22ClF3N6O3
Molecular Weight: 546.9287896000001
MDL Number: MFCD20528907
SMILES: Nc1nc(cc(n1)c1ccc(cc1)C[C@@H](C(=O)O)N)O[C@@H](C(F)(F)F)c1ccc(cc1n1ccc(n1)C)Cl

 

Upstream Synthesis Route
  • The compound $name$ plays a crucial role in chemical synthesis as a key building block for the creation of pharmaceutical compounds. Its unique structure consisting of an amino group, trifluoroethoxy group, pyrimidine ring, and phenylalanine moiety makes it a versatile intermediate in the synthesis of various biologically active molecules.In chemical synthesis, $name$ can be utilized as a starting material for the production of novel drugs or drug variants. The presence of the amino group allows for facile derivatization, enabling the attachment of different functional groups to modulate the compound's pharmacological properties. Additionally, the trifluoroethoxy group can serve as a protecting group in organic synthesis, safeguarding specific functional groups from undesired reactions and facilitating selective transformations.Furthermore, the pyrimidine ring in $name$ imparts structural diversity and potential for bioactivity in the synthesized molecules. By incorporating this heterocyclic motif, chemists can explore new chemical space and potentially discover compounds with improved therapeutic effects. Coupled with the phenylalanine unit, which provides chirality and potential protein-binding interactions, $name$ presents a valuable tool for designing and synthesizing biologically active compounds with precision and efficacy in chemical synthesis.
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