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Catalog Number:
41504
CAS Number:
198646-60-5
Acide ( S )-1-Boc-4-oxopipéridine-2-carboxylique
Purity:
94 - 105 % (dosage par titrage)
Synonym(s):
Acide (2 S )-1-Boc-4-oxopipécolique
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Product Information

Adapté à la synthèse de peptides

Synonyms
Acide (2 S )-1-Boc-4-oxopipécolique
CAS Number
198646-60-5
Purity
94 - 105 % (dosage par titrage)
Molecular Formula
C 11 H 175
Molecular Weight
243.26
MDL Number
MFCD03094867
PubChem ID
46835694
Melting Point
121 - 125 °C
Appearance
Solide blanc à blanc cassé
Optical Rotation
[ á]22/D = -18,5 ° (C = 1 dans le chloroforme)
Conditions
Magasin chez RT
General Information
Synonyms
Acide (2 S )-1-Boc-4-oxopipécolique
CAS Number
198646-60-5
Purity
94 - 105 % (dosage par titrage)
Molecular Formula
C 11 H 175
Molecular Weight
243.26
MDL Number
MFCD03094867
PubChem ID
46835694
Melting Point
121 - 125 °C
Appearance
Solide blanc à blanc cassé
Optical Rotation
[ á]22/D = -18,5 ° (C = 1 dans le chloroforme)
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-1-Boc-4-oxopiperidine-2-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 in the development of analgesics and anti-inflammatory drugs.
  • Peptide Synthesis: It is commonly used in peptide synthesis, enhancing the stability and bioavailability of peptide-based therapeutics, which is crucial for drug efficacy.
  • Research in Neuroscience: The compound is valuable in neuroscience research, where it aids in the design of compounds that can modulate neurotransmitter systems, potentially leading to new treatments for neurological disorders.
  • Organic Synthesis: It acts as a versatile building block in organic synthesis, allowing chemists to create complex molecules efficiently, which is essential in both academic and industrial settings.
  • Bioconjugation Techniques: This chemical is utilized in bioconjugation techniques, facilitating the attachment of biomolecules to drugs or imaging agents, thereby improving targeted delivery systems in medical applications.

Citations