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Catalog Number:
16010
CAS Number:
1049734-02-2
Chlorhydrate d'acide ±)- trans -4-(4-nitrophényl)pyrrolidine-3-carboxylique
Synonym(s):
trans -DL-β-Pro-4-(4-nitrophényl)-OH·HCl
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$120.88 /25 mg
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Product Information

(±)-trans-4-(4-Nitrophenyl)pyrrolidine-3-carboxylic acid hydrochloride is a versatile compound with significant applications in pharmaceutical research and development. This compound, often recognized for its role as a building block in the synthesis of various biologically active molecules, exhibits unique properties that make it valuable in medicinal chemistry. Its nitrophenyl group enhances its reactivity, allowing for the development of novel therapeutic agents, particularly in the fields of neuropharmacology and anti-inflammatory research.

Researchers have utilized this compound in the design of selective inhibitors and modulators, contributing to advancements in drug discovery. Its hydrochloride form ensures improved solubility, facilitating easier handling and incorporation into formulations. With its potential to serve as a precursor for more complex structures, (±)-trans-4-(4-Nitrophenyl)pyrrolidine-3-carboxylic acid hydrochloride stands out as an essential tool for scientists aiming to innovate in drug development and therapeutic applications.

Synonyms
trans -DL-β-Pro-4-(4-nitrophényl)-OH·HCl
CAS Number
1049734-02-2
Molecular Formula
C11H12N2O4 · HCl
Molecular Weight
272.69
MDL Number
MFCD06659278
PubChem ID
53398070
Conditions
Conserver à 0-8°C
General Information
Synonyms
trans -DL-β-Pro-4-(4-nitrophényl)-OH·HCl
CAS Number
1049734-02-2
Molecular Formula
C11H12N2O4 · HCl
Molecular Weight
272.69
MDL Number
MFCD06659278
PubChem ID
53398070
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(±)-trans-4-(4-Nitrophenyl)pyrrolidine-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 developing drugs targeting neurological disorders due to its ability to modulate neurotransmitter activity.
  • Biochemical Research: It is used in studies investigating enzyme inhibition and receptor binding, helping researchers understand complex biological pathways and develop new therapeutic strategies.
  • Material Science: The compound is explored for its potential in creating novel materials with specific electronic properties, which can be beneficial in the development of sensors and organic electronics.
  • Analytical Chemistry: It acts as a standard in chromatographic techniques, allowing for the accurate quantification of similar compounds in various samples, thus enhancing the reliability of analytical results.
  • Academic Research: This chemical is frequently employed in educational settings for organic synthesis experiments, providing students with hands-on experience in chemical reactions and compound characterization.

Citations