(R)-Amino-(4-Hydroxyphenyl)Acetic Acid Methyl Ester Hydrochloride

98%

  • Product Code: 76392
  Alias:    (R)-Amino-(4-hydroxyphenyl)acetate methyl ester hydrochloride p-hydroxyphenylglycine methyl ester hydrochloride D-A-(6-methyl-4-hydroxynicotinamide)-P-hydroxyphenyl Ethyl acetate (R)-amino-(4-hydroxyphenyl)methyl acetate hydrochloride
  CAS:    57591-61-4
Molecular Weight: 217.65 g./mol Molecular Formula: C₉H₁₂ClNO₃
EC Number: MDL Number: MFCD01862152
Melting Point: 187-190 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug production. Its structure makes it valuable for creating enantiomerically pure compounds, which are crucial in designing medications with specific biological activities and reduced side effects. It is often employed in the preparation of β-lactam antibiotics and other therapeutic agents targeting bacterial infections. Additionally, its role in asymmetric synthesis supports the production of high-purity active pharmaceutical ingredients (APIs) for improved drug efficacy and safety.
Product Specification:
Test Specification
APPEARANCE White to Tan Powder,Crystals,Granules and/or Chunk
PURITY 97.5-100
CARBON 47.9 % 51.4 %
Infrared spectrum Conforms to Structure
NITROGEN 6.2 % 6.7 %
PROTON NMR SPECTRUM Conforms to Structure
Specific rotation 20Dc 1.0 1N HCl -110
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿420.00
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-
25.000 10-20 days ฿900.00
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-
100.000 10-20 days ฿2,480.00
+
-
500.000 10-20 days ฿11,850.00
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-
(R)-Amino-(4-Hydroxyphenyl)Acetic Acid Methyl Ester Hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug production. Its structure makes it valuable for creating enantiomerically pure compounds, which are crucial in designing medications with specific biological activities and reduced side effects. It is often employed in the preparation of β-lactam antibiotics and other therapeutic agents targeting bacterial infections. Additionally, its role in asymmetric synthesis supports the production of high-purity active pharmaceutical ingredients (APIs) for improved drug efficacy and safety.
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