08011
(R)-2-Vinyloxirane
≥95.0% (sum of enantiomers, GC)
Synonym(s):
(R)-3,4-Epoxy-1-butene
Sign In to View Organizational & Contract Pricing.
About This Item
Empirical Formula (Hill Notation):
C4H6O
CAS Number:
Molecular Weight:
70.09
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5238465
UNSPSC Code:
12352005
NACRES:
NA.22
Skip To
Product Name
(R)-2-Vinyloxirane, ≥95.0% (sum of enantiomers, GC)
InChI
1S/C4H6O/c1-2-4-3-5-4/h2,4H,1,3H2/t4-/m1/s1
SMILES string
C=C[C@@H]1CO1
InChI key
GXBYFVGCMPJVJX-SCSAIBSYSA-N
assay
≥95.0% (sum of enantiomers, GC)
form
liquid
optical activity
[α]20/D −21.0±1°, c = 1% in pentane(lit.)
[α]20/D −21.0±1°, c = 1% in pentane
refractive index
n20/D 1.417
bp
66 °C (lit.)
density
0.870 g/mL at 20 °C (lit.)
storage temp.
2-8°C
Quality Level
Other Notes
Used to prepare stereodiversified scaffolds in library synthesis[1]
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Tiffany Malinky Gierasch et al.
Organic letters, 5(5), 621-624 (2003-02-28)
The syntheses of stereodiverse libraries of 12 and 19 are reported, where each asterisk represents an independently varied stereocenter. These scaffolds provide additional templates for investigations of geometric diversity in library syntheses. Libraries of these N-Fmoc-amino acids were further functionalized
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service