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Catalog Number:
16553
CAS Number:
367966-41-4
Éster metílico de Boc-4( R )-hidroxi-5-oxo-L-prolina
Purity:
≥ 98% (RMN)
Synonym(s):
1- tert -Butil 2-metil(2 S ,4 R )-4-hidroxi-5-oxopirrolidin-1,2-dicarboxilato
Temperature Sensitive
Documents
$140.00 /25 mg
Tamaño
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Product Information

Boc-4-hydroxy-5-oxo-L-proline methyl ester is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This compound, also known as tert-butyl 4-hydroxy-5-oxoproline methyl ester, serves as a valuable building block for the synthesis of various bioactive molecules, particularly in the development of peptide-based therapeutics. Its unique structure, featuring both a Boc (tert-butoxycarbonyl) protecting group and a methyl ester, enhances its stability and reactivity, making it an ideal candidate for coupling reactions and other synthetic transformations.

Researchers and industry professionals appreciate Boc-4-hydroxy-5-oxo-L-proline methyl ester for its ability to facilitate the creation of complex molecular architectures. Its application extends to the synthesis of amino acid derivatives and peptidomimetics, which are crucial in drug discovery and development. The compound's favorable properties, such as its solubility and compatibility with various reaction conditions, position it as a preferred choice for those looking to innovate in medicinal chemistry and related fields.

Synonyms
1- tert -Butil 2-metil(2 S ,4 R )-4-hidroxi-5-oxopirrolidin-1,2-dicarboxilato
CAS Number
367966-41-4
Purity
≥ 98% (RMN)
Molecular Formula
C 11 H 17 N º 6
Molecular Weight
259.26
MDL Number
MFCD08274462
PubChem ID
71437348
Appearance
Blanco rosado o sólido blanco
Optical Rotation
[a] D 20 = 19 ± 2 º (C=1 en CHCl 3 )
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
1- tert -Butil 2-metil(2 S ,4 R )-4-hidroxi-5-oxopirrolidin-1,2-dicarboxilato
CAS Number
367966-41-4
Purity
≥ 98% (RMN)
Molecular Formula
C 11 H 17 N º 6
Molecular Weight
259.26
MDL Number
MFCD08274462
PubChem ID
71437348
Appearance
Blanco rosado o sólido blanco
Optical Rotation
[a] D 20 = 19 ± 2 º (C=1 en CHCl 3 )
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-4-hydroxy-5-oxo-L-proline methyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of bioactive compounds and pharmaceuticals.
  • Drug Development: It plays a crucial role in the design of new drugs, especially those targeting neurological disorders, due to its structural properties that mimic natural amino acids.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing for the attachment of drugs to antibodies or other biomolecules, enhancing targeted delivery in therapies.
  • Research in Metabolism: It aids researchers in studying metabolic pathways and enzyme interactions, providing insights into how certain compounds are processed in the body.
  • Cosmetic Formulations: The compound is also explored in cosmetic science for its potential benefits in skin care products, particularly for its moisturizing and anti-aging properties.

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