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Catalog Number:
15663
CAS Number:
757937-66-9
S-3-Amino-3-(2,4-dichlorophenyl)propionic acid
Purity:
≥ 98% (HPLC, Chiral purity)
Synonym(s):
L-β-Phe(2,4-DiCl)-OH, (S-2,4-Dichloro-β-phenylalanine
Documents
$72.31 /250MG
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Product Information

(S)-3-Amino-3-(2,4-dichlorophenyl)propionic acid is a versatile compound with significant applications in pharmaceutical research and development. This amino acid derivative is recognized for its potential as a building block in the synthesis of various bioactive molecules, particularly in the field of medicinal chemistry. Its unique structure, featuring a dichlorophenyl group, enhances its ability to interact with biological systems, making it a valuable candidate for drug discovery and development. Researchers have explored its role in modulating neurotransmitter systems, which could lead to advancements in treatments for neurological disorders.

In addition to its pharmaceutical applications, (S)-3-Amino-3-(2,4-dichlorophenyl)propionic acid can also serve as a useful reagent in organic synthesis, facilitating the creation of complex molecules with specific functionalities. Its stability and reactivity make it an ideal choice for researchers looking to develop new compounds with targeted therapeutic effects. With its promising profile, this compound stands out as a key ingredient in the ongoing quest for innovative solutions in both research and industry.

Synonyms
L-β-Phe(2,4-DiCl)-OH, (S-2,4-Dichloro-β-phenylalanine
CAS Number
757937-66-9
Purity
≥ 98% (HPLC, Chiral purity)
Molecular Formula
C9H9Cl2NO2
Molecular Weight
234.08
MDL Number
MFCD04113673
PubChem ID
600035
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
L-β-Phe(2,4-DiCl)-OH, (S-2,4-Dichloro-β-phenylalanine
CAS Number
757937-66-9
Purity
≥ 98% (HPLC, Chiral purity)
Molecular Formula
C9H9Cl2NO2
Molecular Weight
234.08
MDL Number
MFCD04113673
PubChem ID
600035
Appearance
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

(S)-3-Amino-3-(2,4-dichlorophenyl)propionic acid 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 with improved efficacy and reduced side effects.
  • Biochemical Research: Researchers use this compound to study amino acid metabolism and its effects on cellular processes. Its role in modulating neurotransmitter activity makes it valuable in understanding brain function and related diseases.
  • Agricultural Chemistry: The compound is explored for its potential as a plant growth regulator, helping to enhance crop yields and resistance to pests. This application can lead to more sustainable agricultural practices.
  • Analytical Chemistry: It is utilized as a standard in various analytical methods, including chromatography, to ensure accurate measurement of related compounds in complex mixtures.
  • Material Science: The compound is investigated for its potential use in developing new materials with specific properties, such as improved thermal stability and mechanical strength, beneficial for various industrial applications.

Citations