408409
trans-N-(2-Furfurylideneacetyl)glycine
98%
Synonym(s):
N-[(2E)-3-(2-Furanyl)-1-oxo-2-propen-1-yl]-glycine
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About This Item
Empirical Formula (Hill Notation):
C9H9NO4
CAS Number:
Molecular Weight:
195.17
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
Assay
98%
mp
218-221 °C (lit.)
application(s)
peptide synthesis
SMILES string
OC(=O)CNC(=O)\C=C\c1ccco1
InChI
1S/C9H9NO4/c11-8(10-6-9(12)13)4-3-7-2-1-5-14-7/h1-5H,6H2,(H,10,11)(H,12,13)/b4-3+
InChI key
XJVSWKBQMAOKAX-ONEGZZNKSA-N
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A Kanstrup et al.
Analytical biochemistry, 194(1), 41-44 (1991-04-01)
Furylacryloyl substrates used in kinetic measurements of proteolytic enzymes are shown to cis-trans photoisomerize quickly in plain daylight. The enzymatic transformation of the two forms is sufficiently different to cause problems for such measurements without careful protection against light.
M K Parkash et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 32(10), 887-895 (1994-10-01)
The fate of furfural (2-furancarboxaldehyde) was investigated in male and female Fischer 344 (F344) rats given single oral doses of 1, 10 and 60 mg/kg and male and female CD1 mice given 1, 20 and 200 mg/kg [carbonyl-14C]furfural. There was
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