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2,2-Diphenylglycine, 98%, Thermo Scientific Chemicals
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Catalog number B22650.06
also known as B22650-06
Price (USD)/ Each
82.65
Online exclusive
91.20 Save 8.55 (9%)
-
Quantity:
5 g
Price (USD)/ Each
82.65
Online exclusive
91.20 Save 8.55 (9%)
2,2-Diphenylglycine, 98%, Thermo Scientific Chemicals
Catalog numberB22650.06
Price (USD)/ Each
82.65
Online exclusive
91.20 Save 8.55 (9%)
-
Chemical Identifiers
CAS3060-50-2
Specifications
Specification Sheet
Specification SheetAppearance (Color)White
FormPowder
Assay (Non-aqueous acid-base Titration)≥97.5 to ≤102.5%
2,2-Diphenylglycine is used as a synthesis reagent for amination reactions. It acts as an intermediate in pharmaceutical and in organic synthesis.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,2-Diphenylglycine is used as a synthesis reagent for amination reactions. It acts as an intermediate in pharmaceutical and in organic synthesis.
Solubility
It is sparingly soluble in water.
Notes
Incompatible with oxidizing agents.
2,2-Diphenylglycine is used as a synthesis reagent for amination reactions. It acts as an intermediate in pharmaceutical and in organic synthesis.
Solubility
It is sparingly soluble in water.
Notes
Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Ding, L.; Chen, J.; Hu, Y.; Xu, J.; Gong, X.; Xu, D.; Zhao, B.; Li, H. Aminative Umpolung of Aldehydes to α-Amino Anion Equivalents for Pd-Catalyzed Allylation: An Efficient Synthesis of Homoallylic Amine. Org. Lett.. 2014, 16 (3), 720-723.
- Liu, X.; Gao, A.; Ding, L.; Xu, J.; Zhao, B. Aminative Umpolung Synthesis of Aryl Vicinal Diamines from Aromatic Aldehydes. Org. Lett. 2014, 16 (8), 2118-2121.
- Chen, T.; Yang, L.; Gong, D.; Huang, K-W. Synthesis, crystal structure and reactivity studies of iron complexes with pybox ligands. Inorg. Chim. Acta. 2014, 423, 320-325.
- Tang, S.; Park, Y. J.; Yeagley, A. A.; Sabat, M.; Chruma, J. J. Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction. Org. Lett. 2015, 17 (9), 2042-2045.