D-2-Phenylglycine

95%

  • Product Code: 105747
  Alias:    L-phenylglycine; D-2-phenylglycine
  CAS:    875-74-1
Molecular Weight: 151.16 g./mol Molecular Formula: C₈H₉NO₂
EC Number: 212-876-3 MDL Number: MFCD00008061
Melting Point: 302 °C (dec.)(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: D-2-Phenylglycine is widely used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-lactam antibiotics such as semisynthetic penicillins and cephalosporins. It serves as a key intermediate in the manufacture of amoxicillin and cefaclor, contributing to their antibacterial properties. Additionally, it is employed in the preparation of other bioactive compounds, including peptidomimetics and enzyme inhibitors, due to its ability to introduce chirality into molecules. Its role in asymmetric synthesis also makes it valuable in the development of enantiomerically pure drugs, enhancing their efficacy and reducing side effects.
Product Specification:
Test Specification
Purity (%) 94.5-100
Solubility In 1Mol/L NaOH Almost Transparency
Infrared Spectrum Conforms To Structure
Specific Rotation [A]20/D(C=1 In 1N HCl) -158-154
UV Absorption λ: 420 Nm A 0-0.03
Water By Karl Fischer 0-0.1
Appearance White To Off-White Powder Or Crystals
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
25.000 10-20 days ฿620.00
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-
100.000 10-20 days ฿1,070.00
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-
500.000 10-20 days ฿3,770.00
+
-
2500.000 10-20 days ฿11,320.00
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-
D-2-Phenylglycine
D-2-Phenylglycine is widely used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-lactam antibiotics such as semisynthetic penicillins and cephalosporins. It serves as a key intermediate in the manufacture of amoxicillin and cefaclor, contributing to their antibacterial properties. Additionally, it is employed in the preparation of other bioactive compounds, including peptidomimetics and enzyme inhibitors, due to its ability to introduce chirality into molecules. Its role in asymmetric synthesis also makes it valuable in the development of enantiomerically pure drugs, enhancing their efficacy and reducing side effects.
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