(S)-(-)-2-Amino-4-pentenoic acid

98%

  • Product Code: 60758
  Alias:    (S)-(-)-2-Amino-4-pentenoic acid; L-alpha-allylglycine
  CAS:    16338-48-0
Molecular Weight: 115.13 g./mol Molecular Formula: C₅H₉NO₂
EC Number: MDL Number: MFCD00002627
Melting Point: 283 °C (dec.)(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: (S)-(-)-2-Amino-4-pentenoic acid is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active compounds, including peptides and enzyme inhibitors. Its unique structure allows it to participate in reactions that form carbon-carbon and carbon-nitrogen bonds, making it valuable in the development of new drugs. Additionally, it is employed in the study of metabolic pathways and as a building block for the synthesis of chiral molecules, which are crucial in the creation of enantiomerically pure pharmaceuticals. Its application extends to biochemical research, where it is used to investigate amino acid metabolism and enzyme mechanisms.
Product Specification:
Test Specification
ENANTIOMERIC EXCESS GC 98-100
PURITYHPLC 98 100%
SPECIFIC ROTATION A20DC4 WATER -35 -39
APPEARANCE WHITE TO LIGHT YELLOW POWDER
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿400.00
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-
1.000 10-20 days ฿1,490.00
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-
5.000 10-20 days ฿5,060.00
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(S)-(-)-2-Amino-4-pentenoic acid
(S)-(-)-2-Amino-4-pentenoic acid is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various biologically active compounds, including peptides and enzyme inhibitors. Its unique structure allows it to participate in reactions that form carbon-carbon and carbon-nitrogen bonds, making it valuable in the development of new drugs. Additionally, it is employed in the study of metabolic pathways and as a building block for the synthesis of chiral molecules, which are crucial in the creation of enantiomerically pure pharmaceuticals. Its application extends to biochemical research, where it is used to investigate amino acid metabolism and enzyme mechanisms.
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