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等级
puriss.
方案
≥99.0% (AT)
灼烧残渣
≤0.05%
mp
175 °C (dec.) (lit.)
175-176 °C (dec.)
SMILES字符串
Cl.COC(=O)CN
InChI
1S/C3H7NO2.ClH/c1-6-3(5)2-4;/h2,4H2,1H3;1H
InChI key
COQRGFWWJBEXRC-UHFFFAOYSA-N
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Glycine enolates: the large effect of iminium ion formation on alpha-amino carbon acidity.
A Rios et al.
Journal of the American Chemical Society, 123(32), 7949-7950 (2001-08-09)
Inactivation of chicken muscle enolase by carbodiimide and glycine methyl ester.
G A Russell et al.
FEBS letters, 143(2), 211-212 (1982-07-05)
Wenzhong Gao et al.
Organic letters, 7(19), 4241-4244 (2005-09-09)
[reaction: see text] A novel Cu(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with acrylates has been developed. Up to 98/2 exo/endo selectivity and up to 98% enantiomeric excess have been achieved.
Akihiko Tohri et al.
European journal of biochemistry, 271(5), 962-971 (2004-03-11)
To elucidate the domains on the extrinsic 23 kDa protein involved in electrostatic interaction with the extrinsic 33 kDa protein in spinach photosystem II, we modified amino or carboxyl groups of the 23 kDa protein to uncharged methyl ester groups
D Solís et al.
Analytical biochemistry, 209(1), 117-122 (1993-02-15)
The usefulness of ricin as a research tool is handicapped by its extremely biohazardous nature. In this work, ricin toxicity has been reduced by chemical modification of carboxyl groups using 1-ethyl-3(3-dimethylaminopropyl) carbodiimide and [14C]glycine methyl ester. The reaction was carried
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