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N-Boc-O-tert-butyl-L-tyrosine, 98%, Thermo Scientific Chemicals
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Catalog number H62801.06
also known as H62801-06
Price (USD)/ Each
143.00
-
Quantity:
5 g
Price (USD)/ Each
143.00
N-Boc-O-tert-butyl-L-tyrosine, 98%, Thermo Scientific Chemicals
Catalog numberH62801.06
Price (USD)/ Each
143.00
-
Chemical Identifiers
CAS47375-34-8
IUPAC Name(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-[4-(tert-butoxy)phenyl]propanoic acid
Molecular FormulaC18H27NO5
InChI KeyZEQLLMOXFVKKCN-YQTOOIBONA-N
SMILESCC(C)(C)OC(=O)N[C@@H](CC1=CC=C(OC(C)(C)C)C=C1)C(O)=O
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)>97.5%
N-Boc-O-tert-butyl-L-tyrosine is used as pharmaceutical intermediate.
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
N-Boc-O-tert-butyl-L-tyrosine is used as pharmaceutical intermediate.
Solubility
Soluble in DMF. Insoluble in water.
Notes
Store in a cool, dry place, in a well sealed container. Store away from oxidizing agents, heat.
N-Boc-O-tert-butyl-L-tyrosine is used as pharmaceutical intermediate.
Solubility
Soluble in DMF. Insoluble in water.
Notes
Store in a cool, dry place, in a well sealed container. Store away from oxidizing agents, heat.
RUO – Research Use Only
General References:
- V. F. Pozdnev; M. Yu. Chernaya. Activation of a carboxy group by dialkyl pyrocarbonates. Synthesis of symmetrical anhydrides and aryl esters of N-protected amino acids using di-tert-butyl pyrocarbonate as condensing reagent. Chemistry of Natural Compounds. 1984, 20 (3) 333-337.
- Xiaorui Wang; Jinming Hu; Guoying Zhang and Shiyong Liu. Highly Selective Fluorogenic Multianalyte Biosensors Constructed via Enzyme-Catalyzed Coupling and Aggregation-Induced Emission. J. Am. Chem. Soc. 2014, 136 (28), 9890-9893.