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Catalog Number:
14391
CAS Number:
14091-11-3
DL-Phe(2-Cl)-OH
Purity:
≥ 99% (HPLC)
Synonym(s):
2-Chloro-DL-phenylalanine, o-Chloro-DL-phenylalanine, (RS-2-Amino-3-(2-chlorphenyl)propionic acid
Documents
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Product Information

DL-Phe(2-Cl)-OH, also known as 2-amino-3-(2-chlorophenyl)propanoic acid, is a versatile compound widely utilized in pharmaceutical and biochemical research. This amino acid derivative features a chlorophenyl group that enhances its reactivity and potential applications in drug development. Researchers often leverage DL-Phe(2-Cl)-OH in the synthesis of various bioactive molecules, particularly in the design of novel therapeutic agents targeting neurological disorders. Its unique structure allows for modifications that can lead to compounds with improved efficacy and selectivity.

In addition to its role in medicinal chemistry, DL-Phe(2-Cl)-OH is also valuable in the study of protein interactions and enzyme activity, making it an essential tool for biochemists and molecular biologists. The compound's ability to mimic natural amino acids while providing distinct functional properties makes it a preferred choice for researchers aiming to explore new biochemical pathways or develop innovative treatments. With its broad applicability and significant potential, DL-Phe(2-Cl)-OH stands out as a crucial compound in advancing scientific research and pharmaceutical development.

Synonyms
2-Chloro-DL-phenylalanine, o-Chloro-DL-phenylalanine, (RS-2-Amino-3-(2-chlorphenyl)propionic acid
CAS Number
14091-11-3
Purity
≥ 99% (HPLC)
Molecular Formula
C9H10ClNO2
Molecular Weight
199.6
MDL Number
MFCD00037774
PubChem ID
85679
Melting Point
230-236 °C
Conditions
Store at 0-8°C
General Information
Synonyms
2-Chloro-DL-phenylalanine, o-Chloro-DL-phenylalanine, (RS-2-Amino-3-(2-chlorphenyl)propionic acid
CAS Number
14091-11-3
Purity
≥ 99% (HPLC)
Molecular Formula
C9H10ClNO2
Molecular Weight
199.6
MDL Number
MFCD00037774
PubChem ID
85679
Melting Point
230-236 °C
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

DL-Phe(2-Cl)-OH is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders. Its unique structure allows for the development of drugs that can effectively interact with neurotransmitter systems.
  • Biochemical Research: Researchers use DL-Phe(2-Cl)-OH to study protein interactions and enzyme activities. Its ability to mimic natural amino acids makes it valuable in understanding metabolic pathways and protein synthesis.
  • Agrochemicals: The compound is explored in the formulation of herbicides and pesticides, providing enhanced efficacy against specific plant species while minimizing environmental impact, which is crucial for sustainable agriculture.
  • Material Science: In polymer chemistry, DL-Phe(2-Cl)-OH is incorporated into biopolymers to improve their mechanical properties and biodegradability, making it beneficial for developing eco-friendly materials.
  • Diagnostic Applications: This chemical is also researched for its potential use in diagnostic assays, particularly in detecting specific biomarkers related to certain diseases, offering a promising avenue for early diagnosis and treatment.

Citations