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Catalog Number:
16021
CAS Number:
1381947-36-9
Ácido Boc-(±)- trans -4-(2-trifluorometilfenil)pirrolidin-3-carboxílico
Purity:
≥ 95%
Synonym(s):
Boc- trans -DL-β-Pro-4-(2-trifluorometilfenil)-OH
Documents
$79.22 /100 mg
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Product Information

Boc-(±)-trans-4-(2-trifluoromethylphenyl)pyrrolidine-3-carboxylic acid is a versatile compound widely utilized in pharmaceutical research and development. This compound features a unique trifluoromethyl group, which enhances its biological activity and selectivity, making it an attractive candidate for drug design and synthesis. Its Boc (tert-butyloxycarbonyl) protecting group allows for straightforward manipulation in organic synthesis, facilitating the development of complex molecules. Researchers often leverage this compound in the synthesis of novel pharmaceuticals, particularly in the creation of potent inhibitors and modulators in various therapeutic areas, including neuropharmacology and oncology.

The compound's distinct structural characteristics contribute to its effectiveness in medicinal chemistry, where it serves as a building block for more complex structures. Its application in the synthesis of pyrrolidine derivatives has shown promise in enhancing the efficacy of drug candidates. With its favorable properties, Boc-(±)-trans-4-(2-trifluoromethylphenyl)pyrrolidine-3-carboxylic acid stands out as a valuable tool for researchers aiming to innovate and develop new therapeutic agents.

Synonyms
Boc- trans -DL-β-Pro-4-(2-trifluorometilfenil)-OH
CAS Number
1381947-36-9
Purity
≥ 95%
Molecular Formula
C17H20F3NO4
Molecular Weight
359.34
MDL Number
MFCD06659289
PubChem ID
45074059
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc- trans -DL-β-Pro-4-(2-trifluorometilfenil)-OH
CAS Number
1381947-36-9
Purity
≥ 95%
Molecular Formula
C17H20F3NO4
Molecular Weight
359.34
MDL Number
MFCD06659289
PubChem ID
45074059
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(±)-trans-4-(2-trifluoromethylphenyl)pyrrolidine-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Organic Synthesis: It is employed in organic synthesis as a building block for creating complex molecules, allowing chemists to explore new chemical entities with potential therapeutic effects.
  • Material Science: The compound can be used in the formulation of advanced materials, contributing to the development of polymers with enhanced properties for industrial applications.
  • Research in Medicinal Chemistry: It plays a significant role in medicinal chemistry research, aiding scientists in understanding structure-activity relationships (SAR) for drug design.
  • Fluorinated Compound Research: Given its trifluoromethyl group, it is valuable in studies exploring the effects of fluorination on biological activity, offering insights into the design of more effective compounds.

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