Type: | Sodium Organic Salt |
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Appearance: | Powder |
Grade Standard: | Food Grade |
Product Name: | D-2-Phenylglycine |
CAS Number: | 875-74-1 |
Molecular Weight: | 151.163 |
Customization: |
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Common Name | D-2-Phenylglycine | ||
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CAS Number | 875-74-1 | Molecular Weight | 151.163 |
Density | 1.2±0.1 g/cm3 | Boiling Point | 288.7±28.0 °C at 760 mmHg |
Molecular Formula | C8H9NO2 | Melting Point | 302ºC |
MSDS | ChineseUSA | Flash Point | 128.4±24.0 °C |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 288.7±28.0 °C at 760 mmHg |
Melting Point | 302ºC |
Molecular Formula | C8H9NO2 |
Molecular Weight | 151.163 |
Flash Point | 128.4±24.0 °C |
Exact Mass | 151.063324 |
PSA | 63.32000 |
LogP | 0.94 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.589 |
D-2-phenylglycine, also known as D-α-phenylglycine or D-(+)-2-phenylglycine, is an organic compound with the molecular formula C8H9NO2. It is an amino acid derivative that contains a phenyl group attached to the alpha carbon of the glycine molecule.
Stereochemistry: D-2-phenylglycine belongs to the D-enantiomer class, meaning it has a specific three-dimensional arrangement of atoms that corresponds to the D configuration. The D-enantiomer is the mirror image of the L-enantiomer, which has the opposite configuration.
Synthetic applications: D-2-phenylglycine is commonly used as a chiral building block in organic synthesis. Its unique structure and stereochemistry make it a valuable precursor for the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals.
Pharmaceutical applications: D-2-phenylglycine serves as a key intermediate in the production of several important drugs. It is used in the synthesis of certain antibiotics, such as penicillins and cephalosporins, where it acts as a precursor for the formation of the beta-lactam ring.
Asymmetric synthesis: Due to its chiral nature, D-2-phenylglycine is often utilized in the asymmetric synthesis of other compounds. It can be employed as a chiral auxiliary or ligand to induce chirality in reactions and obtain enantiomerically pure products.
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