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N-Boc-L-aspartic acid 4-tert-butyl ester, 98%, Thermo Scientific Chemicals
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Catalog number H63554.06
also known as H63554-06
Price (USD)/ Each
53.90
-
Quantity:
5 g
Price (USD)/ Each
53.90
N-Boc-L-aspartic acid 4-tert-butyl ester, 98%, Thermo Scientific Chemicals
Catalog numberH63554.06
Price (USD)/ Each
53.90
-
Chemical Identifiers
CAS1676-90-0
IUPAC Name4-(tert-butoxy)-2-{[(tert-butoxy)carbonyl]amino}-4-oxobutanoic acid
Molecular FormulaC13H23NO6
InChI KeyPHJDCONJXLIIPW-UHFFFAOYNA-N
SMILESCC(C)(C)OC(=O)CC(NC(=O)OC(C)(C)C)C(O)=O
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)>97.5%
It is used in the preparation of highly selective thrombin inhibitors. Also used in the preparation of thiopeptides and thioacylating agents.
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
It is used in the preparation of highly selective thrombin inhibitors. Also used in the preparation of thiopeptides and thioacylating agents.
Solubility
Soluble in methanol and dimethyl sulfoxide.
Notes
Refrigerate. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
It is used in the preparation of highly selective thrombin inhibitors. Also used in the preparation of thiopeptides and thioacylating agents.
Solubility
Soluble in methanol and dimethyl sulfoxide.
Notes
Refrigerate. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Kurt Hilpert; Jean Ackermann; David W. Banner; Alain Gast; Klaus Gubernator; Paul Hadvary; Ludvik Labler; Klaus Mueller; Gerard Schmid,. Design and Synthesis of Potent and Highly Selective Thrombin Inhibitors. J. Med. Chem. 1994, 37(23), 3889-3901.
- M. Ashraf Shalaby; Christopher W. Grote; and Henry Rapoport. Thiopeptide Synthesis. α-Amino Thionoacid Derivatives of Nitrobenzotriazole as Thioacylating Agents. J. Org. Chem. 1996, 61(25), 9045-9048.