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Catalog Number:
16740
CAS Number:
264903-49-3
Ácido D-2-amino-4-bromo-4-pentenoico
Purity:
≥ 98 % (TLC)
Documents
$72.31 /100 mg
Tamaño
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Product Information

D-2-Amino-4-bromo-4-pentenoic acid is a versatile compound recognized for its unique properties and potential applications in various fields, particularly in pharmaceutical and biochemical research. This amino acid derivative, characterized by its bromine substitution, serves as a valuable building block in the synthesis of bioactive molecules. Its structural features allow it to participate in diverse chemical reactions, making it an essential component in the development of novel therapeutic agents. Researchers have utilized D-2-Amino-4-bromo-4-pentenoic acid in studies focusing on enzyme inhibition and receptor modulation, highlighting its significance in drug discovery and development.

In addition to its research applications, this compound is also explored for its potential in agricultural chemistry, where it may contribute to the design of new agrochemicals. Its ability to modify biological pathways positions it as a candidate for enhancing crop protection strategies. With its unique properties and broad applicability, D-2-Amino-4-bromo-4-pentenoic acid stands out as a promising tool for researchers and industry professionals seeking innovative solutions in their respective fields.

CAS Number
264903-49-3
Purity
≥ 98 % (TLC)
Molecular Formula
C5H8BrNO2
Molecular Weight
194.03
MDL Number
MFCD06659108
PubChem ID
228809
Melting Point
242-248 °C (descenso)
Appearance
Polvo amarillento
Optical Rotation
[a] D 25 = +21 ± 2º (C=1 en H2O)
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
CAS Number
264903-49-3
Purity
≥ 98 % (TLC)
Molecular Formula
C5H8BrNO2
Molecular Weight
194.03
MDL Number
MFCD06659108
PubChem ID
228809
Melting Point
242-248 °C (descenso)
Appearance
Polvo amarillento
Optical Rotation
[a] D 25 = +21 ± 2º (C=1 en H2O)
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

D-2-Amino-4-bromo-4-pentenoic acid is widely utilized in research focused on:

  • Neuroscience Research: This compound serves as a valuable tool in studying neurotransmitter systems, particularly in understanding the role of amino acids in synaptic transmission.
  • Pharmaceutical Development: It is explored for its potential in developing new drugs targeting neurological disorders, offering a unique structure that may enhance efficacy compared to traditional compounds.
  • Biochemical Assays: The compound is used in various assays to measure enzyme activity, providing insights into metabolic pathways and helping in the discovery of new therapeutic targets.
  • Organic Synthesis: It acts as an intermediate in the synthesis of more complex molecules, facilitating the development of novel chemical entities in medicinal chemistry.
  • Teaching and Education: This compound is often included in academic settings for teaching organic chemistry and biochemistry, helping students understand the principles of amino acid structure and function.

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