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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)
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.
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 physical chemistry. B, 117(10), 2872-2877 (2013-02-15)
In this study, the reactions of presolvated electrons with glycine methyl ester and N-acetylalanylalanine methyl ester (N-aAAMe) are investigated by electron spin resonance (ESR) spectroscopy and DFT calculations. Electrons were produced by γ-irradiation in neutral 7.5 M LiCl-D2O aqueous glasses
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