(S)-Benzyl (1-(1H-benzo[d][1,2,3]triazol-1-yl)-3-(1H-indol-3-yl)-1-oxopropan-2-yl)carbamate structure
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Common Name | (S)-Benzyl (1-(1H-benzo[d][1,2,3]triazol-1-yl)-3-(1H-indol-3-yl)-1-oxopropan-2-yl)carbamate | ||
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CAS Number | 850232-59-6 | Molecular Weight | 439.46600 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C25H21N5O3 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | Cbz-L-Cys(Bz)-Bt |
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Synonym | More Synonyms |
Molecular Formula | C25H21N5O3 |
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Molecular Weight | 439.46600 |
Exact Mass | 439.16400 |
PSA | 101.90000 |
LogP | 4.48140 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
RIDADR | NONH for all modes of transport |
Precursor 0 | |
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DownStream 2 | |
Benzotriazole-mediated syntheses of depsipeptides and oligoesters.
J. Org. Chem. 76 , 4884-4893, (2011) Reactions of O-Pg(α-hydroxyacyl)benzotriazoles with (a) unprotected α-hydroxycarboxylic acids, (b) amino acids, and (c) amines afforded, respectively, chirally pure (a) oligoesters, (b) depsidipeptide... |
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Efficient preparation of aminoxyacyl amides, aminoxy hybrid peptides, and alpha-aminoxy peptides.
J. Org. Chem. 74th ed.,, 8690-8694, (2009) N-(Pg-alpha-aminoxy acids) 1a-g are converted to N-(Pg-alpha-aminoxyacyl)benzotriazoles 2a-g, which react under mild conditions with amines, alpha-amino acids/alpha-dipeptides, and alpha-aminoxy acids... |
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Abdelmajeid, A.; Tala, S. R.; Amine, M. S.; Katritzky, A. R.
Synthesis , 2995-3005, (2011)
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N-Z-L-Trp-Bt |
benzyl N-[(1S)-2-(1H-1,2,3-benzotriazol-1-yl)-1-(1H-indol-3-ylmethyl)-2-oxoethyl]carbamate |
Z-TRP-BT |
Cbz-L-Trp-Bt |
Z-L-Trp-Bt |
(S)-benzyl [1-(1H-benzo[d][1,2,3]triazol-1-yl)-3-(benzylthio)-1-oxopropan-2-yl]carbamate |