Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
22760
CAS Number:
158567-91-0
Ácido 2R , 4R -Boc-4-fenil-pirrolidin-2-carboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
( 2R , 4R- Boc-4-fenil-Pro-OH
Documents
$208.31 /25 mg
Tamaño
Request Bulk Quote
Product Information

(2R,4R)-Boc-4-phenyl-pyrrolidine-2-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound, also known as Boc-4-phenylpyrrolidine-2-carboxylic acid, features a unique structure that allows for effective incorporation into various chemical reactions, particularly in the development of pharmaceuticals. Its Boc (tert-butyloxycarbonyl) protecting group enhances stability and solubility, making it an ideal candidate for peptide synthesis and drug formulation. Researchers appreciate its role in the synthesis of bioactive molecules, where it serves as a key intermediate in the production of potential therapeutic agents targeting neurological disorders.

The compound's chiral centers provide opportunities for creating enantiomerically pure products, which is crucial in the pharmaceutical industry for ensuring efficacy and safety. Its application extends to the synthesis of novel compounds with enhanced biological activity, making it a valuable tool for medicinal chemists. With its favorable properties and practical applications, (2R,4R)-Boc-4-phenyl-pyrrolidine-2-carboxylic acid stands out as a significant asset in both research and industrial settings.

Synonyms
( 2R , 4R- Boc-4-fenil-Pro-OH
CAS Number
158567-91-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C16H21NO4
Molecular Weight
291.35
MDL Number
MFCD09952342
PubChem ID
4712506
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = +32 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
( 2R , 4R- Boc-4-fenil-Pro-OH
CAS Number
158567-91-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C16H21NO4
Molecular Weight
291.35
MDL Number
MFCD09952342
PubChem ID
4712506
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = +32 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2R,4R)-Boc-4-phenyl-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting neurological disorders.
  • Peptide Chemistry: It is commonly used in peptide synthesis, acting as a protecting group for amino acids, which helps in building complex peptide chains with improved yields and purity.
  • Research in Organic Chemistry: The compound is valuable in organic synthesis, allowing chemists to explore new reaction pathways and develop innovative synthetic methodologies.
  • Material Science: Its unique structure enables applications in the development of advanced materials, including polymers with specific mechanical and thermal properties.
  • Biological Studies: Researchers utilize this compound in biological studies to investigate its interactions with various biological targets, aiding in the discovery of new therapeutic agents.

Citas