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Assay
98%
form
solid
optical activity
[α]20/D −8.0°, c = 1.6 in methanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
108-110 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cl.COC(=O)[C@@H](C)N
InChI
1S/C4H9NO2.ClH/c1-3(5)4(6)7-2;/h3H,5H2,1-2H3;1H/t3-;/m1./s1
InChI key
IYUKFAFDFHZKPI-AENDTGMFSA-N
Application
Building block for the preparation of peptides.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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The Journal of Organic Chemistry, 58, 683-683 (1993)
J. Chem. Soc. Perkin Trans. II, 1225-1225 (1992)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(6), 1133-1140 (2005-03-03)
The photophysical properties of 3-[2-(4-diphenylaminophenyl)benzoxazol-5-yl]alanine methyl ester (1b) and its Boc derivative (1a) were studied in a series of solvents. Its UV-Vis absorption spectra are less sensitive to the solvent polarity than the corresponding fluorescence spectra which show pronounced solvatochromic
The Journal of parasitology, 77(2), 187-193 (1991-04-01)
Cultured Schistosoma mansoni schistosomula of various ages were exposed to several lysosomotropic agents. Weak bases such as chloroquine, ammonium chloride, and acridine orange caused gut swelling upon protonation. The latter compound fluoresced a bright orange indicating the acidic nature of
Chemical communications (Cambridge, England), (31)(31), 4675-4677 (2009-07-31)
Femtosecond vibrational pump-probe spectroscopy on beta-helical polyisocyanopeptides reveals vibrational self-trapping in the well-defined hydrogen-bonded side groups that is absent when non-hydrogen bonded monomers are mixed in.
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