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Catalog Number:
16001
CAS Number:
957476-23-2
Ácido Boc-(±)- trans -4-(2-metilfenil)pirrolidin-3-carboxílico
Synonym(s):
Boc- trans -DL-β-Pro-4-(2-metilfenil)-OH
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$72.31 /25 mg
Tamaño
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Product Information

Boc-(±)-trans-4-(2-methylphenyl)pyrrolidine-3-carboxylic acid is a versatile compound widely utilized in the field of medicinal chemistry and pharmaceutical research. This compound serves as a crucial building block in the synthesis of various bioactive molecules, particularly in the development of novel pharmaceuticals targeting neurological disorders and pain management. Its unique structure, featuring a pyrrolidine ring and a Boc (tert-butyloxycarbonyl) protecting group, enhances its stability and solubility, making it an ideal candidate for further functionalization and optimization in drug design.

Researchers appreciate the compound's ability to facilitate the synthesis of complex molecules while maintaining high yields and purity. Its applications extend to the development of chiral intermediates, which are essential in the production of enantiomerically pure drugs. Additionally, the compound's favorable pharmacokinetic properties make it a promising candidate for further exploration in therapeutic applications. With its robust profile, Boc-(±)-trans-4-(2-methylphenyl)pyrrolidine-3-carboxylic acid stands out as a valuable asset for researchers and industry professionals aiming to innovate in drug development.

Synonyms
Boc- trans -DL-β-Pro-4-(2-metilfenil)-OH
CAS Number
957476-23-2
Molecular Formula
C17H23NO4
Molecular Weight
305.37
MDL Number
MFCD06659269
PubChem ID
45074062
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc- trans -DL-β-Pro-4-(2-metilfenil)-OH
CAS Number
957476-23-2
Molecular Formula
C17H23NO4
Molecular Weight
305.37
MDL Number
MFCD06659269
PubChem ID
45074062
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-methylphenyl)pyrrolidine-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Organic Synthesis: It is used in the preparation of complex organic molecules, allowing chemists to create diverse compounds with tailored properties for research and industrial applications.
  • Chiral Catalysis: The compound plays a significant role in asymmetric synthesis, providing researchers with a means to produce chiral molecules that are crucial in the development of effective drugs.
  • Biochemical Research: It is utilized in studies involving enzyme interactions and metabolic pathways, helping scientists understand biological processes and develop new therapeutic strategies.
  • Material Science: The compound is explored in the development of new materials with specific properties, such as polymers and coatings, which can enhance performance in various applications.

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