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Catalog Number:
15885
CAS Number:
129704-91-2
(S-a-Allylproline·HCl
Purity:
≥ 98% (NMR)
Documents
$201.60 /100MG
Pack Size Availability Price
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Product Information

(S)-a-Allylproline·HCl is a valuable compound in the field of organic chemistry, particularly known for its role as a chiral building block in the synthesis of various pharmaceuticals and agrochemicals. This hydrochloride salt form enhances its solubility, making it easier to handle in laboratory settings. Its unique structure allows it to participate in asymmetric synthesis, which is crucial for developing enantiomerically pure compounds. Researchers have utilized (S)-a-Allylproline·HCl in the synthesis of bioactive molecules, including those with potential applications in treating neurological disorders and other therapeutic areas.

This compound stands out due to its ability to facilitate the formation of peptide bonds and its effectiveness in catalyzing reactions that require chirality. Its application extends to the development of novel drug candidates, where the need for specific stereochemistry is paramount. With its proven utility in synthetic methodologies, (S)-a-Allylproline·HCl is an essential reagent for chemists aiming to innovate in drug design and synthesis.

CAS Number
129704-91-2
Purity
≥ 98% (NMR)
Molecular Formula
C8H13NO2·HCl
Molecular Weight
191.66
MDL Number
MFCD06659238
PubChem ID
17750301
Appearance
Off-white powder
Conditions
Store at 0-8°C
General Information
CAS Number
129704-91-2
Purity
≥ 98% (NMR)
Molecular Formula
C8H13NO2·HCl
Molecular Weight
191.66
MDL Number
MFCD06659238
PubChem ID
17750301
Appearance
Off-white powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-a-Allylproline·HCl is widely utilized in research focused on

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Catalysis: It is employed in asymmetric synthesis, where its chiral properties enhance the efficiency of reactions, leading to higher yields of desired enantiomers in drug production.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme mechanisms, providing insights that can lead to new therapeutic strategies.
  • Material Science: Its unique structure allows for the development of novel materials, such as polymers with specific properties for use in coatings and adhesives.
  • Food Industry Applications: The compound can also be explored in flavor chemistry, where it may contribute to the development of new food additives that enhance taste profiles.

Citations