BOC-D- Phenyl glycine
Also known as (2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid, Boc-D-Phg-OH, N-Boc-D-Phenylglycine
- CAS number
- 33125-05-2
- Molecular formula
- C13H17NO4
- Molecular weight
- 251.28 g/mol
- Catalogue number
- OS-18604
- Purity
- 99 %
- Grade
- Industrial
- Form
- Powder
- Packing
- 25 kg
₹8,000 per kg
Documents
- Certificate of analysis (COA) On request
- Safety data sheet (MSDS) On request
Specifications
| CAS number | 33125-05-2 |
|---|---|
| Molecular formula | C13H17NO4 |
| Molecular weight | 251.28 g/mol |
| IUPAC name | (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-phenylacetic acid |
| InChIKey | HOBFSNNENNQQIU-SNVBAGLBSA-N |
| SMILES | CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O |
| MDL number | MFCD00062043 |
| PubChem CID | 2755953 |
| Physical form | Powder |
|---|---|
| Appearance | White Powder |
| Melting point | 233 °C |
| Density | 1.16 g/cm³ |
| Purity | 99 % |
|---|---|
| Grade | Industrial |
| Packaging size | 25 kg |
|---|
Description and applications
N-Boc-D-phenylglycine is an organic compound that is used in the asymmetric synthesis of pyrazoles. It has been shown to react with ketones to form β-unsaturated ketones in a reaction mechanism that involves the formation of an imine intermediate. N-Boc-D-phenylglycine can be synthesized by reacting phenylacetic acid with D,L-alanyl chloride followed by hydrolysis and reaction with ammonia. The compound can also be made from pyrazole and Boc anhydride. N-Boc-D-phenylglycine is soluble in organic solvents such as chloroform and THF but not water, making it useful for organic synthesis under solvent conditions. It is orally bioavailable and can be administered to humans without any toxic effects.
Applications
- protected amino acid
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