Z-L-Prolinol

98%

  • Product Code: 105624
  Alias:    Z-L-Prolinol
  CAS:    6216-63-3
Molecular Weight: 235.28 g./mol Molecular Formula: C₁₃H₁₇NO₃
EC Number: MDL Number: MFCD02683224
Melting Point: Boiling Point: 160 °C0.8 mm Hg(lit.)
Density: 1.196 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: Z-L-Prolinol is widely utilized in the synthesis of pharmaceuticals, particularly in the production of chiral compounds. It serves as a key intermediate in the development of various drugs, including antiviral and anticancer agents. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Additionally, Z-L-Prolinol is employed in peptide chemistry, where it acts as a protecting group for amino acids during peptide bond formation. This ensures the integrity and specificity of the peptide sequence. In organic synthesis, it is also used to construct complex molecular structures, contributing to advancements in medicinal chemistry and drug discovery.
Product Specification:
Test Specification
Purity (HPLC) 97.5-100
Specific Rotation [A]20/D(C=1%, CHCL3) 38-46
Appearance Colorless To Orange Liquid
Proton NMR Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿580.00
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-
5.000 10-20 days ฿2,260.00
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-
25.000 10-20 days ฿10,340.00
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Z-L-Prolinol
Z-L-Prolinol is widely utilized in the synthesis of pharmaceuticals, particularly in the production of chiral compounds. It serves as a key intermediate in the development of various drugs, including antiviral and anticancer agents. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Additionally, Z-L-Prolinol is employed in peptide chemistry, where it acts as a protecting group for amino acids during peptide bond formation. This ensures the integrity and specificity of the peptide sequence. In organic synthesis, it is also used to construct complex molecular structures, contributing to advancements in medicinal chemistry and drug discovery.
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