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Catalog Number:
16062
CAS Number:
1330750-36-1
±)-trans-4-Isopropylpyrrolidine-3-carboxylic acid hydrochloride
Purity:
≥ 98% (NMR)
Synonym(s):
trans-DL-β-Pro-4-(isopropyl)-OH·HCl
Documents
$72.31 /25MG
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Product Information

(±)-trans-4-Isopropylpyrrolidine-3-carboxylic acid hydrochloride is a versatile compound that has garnered attention in various fields, particularly in pharmaceutical research and organic synthesis. This compound, also known as Isopropylpyrrolidine carboxylic acid hydrochloride, exhibits unique structural properties that make it a valuable building block in the synthesis of bioactive molecules. Its chiral nature allows for the development of enantiomerically pure compounds, which are crucial in drug development and formulation.

Researchers have utilized (±)-trans-4-Isopropylpyrrolidine-3-carboxylic acid hydrochloride in the synthesis of novel pharmaceuticals, particularly in the creation of compounds targeting neurological disorders. Its ability to act as a chiral auxiliary enhances its utility in asymmetric synthesis, providing an efficient pathway to produce complex molecules with high stereochemical fidelity. The compound's stability and solubility in various solvents further support its application in laboratory settings, making it an ideal choice for chemists looking to streamline their synthesis processes.

Synonyms
trans-DL-β-Pro-4-(isopropyl)-OH·HCl
CAS Number
1330750-36-1
Purity
≥ 98% (NMR)
Molecular Formula
C8H15NO2·HCl
Molecular Weight
193.67
MDL Number
MFCD06659329
PubChem ID
53398420
Appearance
White to off-white powder
Conditions
Store at 0-8°C
General Information
Synonyms
trans-DL-β-Pro-4-(isopropyl)-OH·HCl
CAS Number
1330750-36-1
Purity
≥ 98% (NMR)
Molecular Formula
C8H15NO2·HCl
Molecular Weight
193.67
MDL Number
MFCD06659329
PubChem ID
53398420
Appearance
White to off-white powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(±)-trans-4-Isopropylpyrrolidine-3-carboxylic acid hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of medications targeting neurological disorders.
  • Biochemical Research: It is used in studies investigating amino acid metabolism and its effects on cellular processes, providing insights into metabolic pathways.
  • Organic Synthesis: The compound is valuable in organic chemistry for creating complex molecules, enhancing the efficiency of synthetic routes in laboratory settings.
  • Chiral Catalysis: Its chiral nature makes it an important reagent in asymmetric synthesis, allowing researchers to produce enantiomerically pure compounds more effectively.
  • Material Science: The compound finds applications in the development of novel materials, particularly in creating polymers with enhanced properties for industrial use.

Citations