Identification
N-alpha-t-Butyloxycarbonyl-N-epsilon-benzyloxycarbonyl-D-lysine
Molecular Formula:
C1 9 H2 8 N2 O6
Synonym:
boc-d-lysine(cbz) ; nalpha-boc-nepsilon-z-d-lysine ; nsc 334941 ; n-alpha-boc-n-epsilon-benzyloxycarbonyl-d-lysine ; n2-[(1,1-dimethylethoxy)carbonyl]-n6-[(phenylmethoxy)carbonyl]-d-lysine ; (r)-6-(((benzyloxy)carbonyl)amino)-2-(((tert-butoxy)carbonyl)amino)-hexanoicacid ; boc-n-epsilon-z-d-lysine ; n-alpha-tert-butyloxycarbonyl-n-epsilon-benzyloxycarbonyl-d-lysine ; d-lysine,n2-[(1,1-dimethylethoxy)carbonyl]-n6-[(phenylmethoxy)carbonyl]- ; boc-d-lysine(z)-oh ; (r)-6-(((benzyloxy)carbonyl)amino)-2-(((tert-butoxy)carbonyl)amino)-hexanoic acid ; n-alpha-butoxycarbonyl-n-epsilon-carbobenzoxy-d-lysine
Description
Building block with side protection orthogonal to Fmoc/tBu strategy. Can be used for side specific derivatization, for example for TFA mediated in situ cyclization, which is taking advantage of intermediate aspartamide formation. Reference: A Tandem In Situ Peptide Cyclization through Trifluoroacetic Acid Cleavage; Koushik Chandra, Tapta Kanchan Roy, Deborah E. Shalev, Abraham Loyter, Chaim Gilon, R. Benny Gerber, and Assaf Friedler; Angew. Chem. Int. Ed. 2014; 53: 9450-9455. DOI: 10.1002/anie.201402789.
Suppliers
Iris Biotech GmbH
BAA1358
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Iris Biotech GmbH
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Suzhou Vosun Biotech Co.,Ltd
SVBC12606300
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AK Scientific, Inc.
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Indofine Chemical Co, Inc.
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Santa Cruz Biotechnology, Inc.
295866
N-alpha-tert-Butyloxycarbonyl-N-epsilon-benzyloxycarbonyl-D-lysine
Iris Biotech GmbH
BAA1358.0005
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Properties
Safety & Transport
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Properties for N-alpha-t-Butyloxycarbonyl-N-epsilon-benzyloxycarbonyl-D-lysine
Molecular Weight:
380.44 g·mol−1
Boiling point:
587°C at 760 mmHg
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Safety & Transport Information
Storage temperature :
Store at RT.
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Alternative Distributors of [N-alpha-t-Butyloxycarbonyl-N-epsilon-benzyloxycarbonyl-D-lysine]
Producers or manufacturers change the product range from time to time.
Currently there are no other manufacturers known.