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

98%

Reagent Code: #60758
label
Alias (S)-(-)-2-Amino-4-pentenoic acid; L-alpha-allylglycine
fingerprint
CAS Number 16338-48-0

science Other reagents with same CAS 16338-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115.13 g/mol
Formula C₅H₉NO₂
badge Registry Numbers
MDL Number MFCD00002627
thermostat Physical Properties
Melting Point 283 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage room temperature

description 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.

format_list_bulleted Product Specification

Test Parameter Specification
Enantiomeric Excess (GC) 98-100
Purity (HPLC) 98-100%
Specific Rotation (A20/D C4 Water) -35 to -39
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,490.00
inventory 5g
10-20 days ฿5,060.00
inventory 250mg
10-20 days ฿400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-(-)-2-Amino-4-pentenoic acid
No image available

(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

(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.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...