516112
Cyclopropylacetonitril
97%
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(2)
About This Item
Lineare Formel:
C3H5CH2CN
CAS-Nummer:
Molekulargewicht:
81.12
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Assay
97%
Brechungsindex
n20/D 1.4235 (lit.)
bp
142-144 °C (lit.)
Dichte
0.878 g/mL at 25 °C (lit.)
SMILES String
N#CCC1CC1
InChI
1S/C5H7N/c6-4-3-5-1-2-5/h5H,1-3H2
InChIKey
FAUQRRGKJKMEIW-UHFFFAOYSA-N
Verwandte Kategorien
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Flam. Liq. 3
Lagerklassenschlüssel
3 - Flammable liquids
WGK
WGK 3
Flammpunkt (°F)
111.0 °F - closed cup
Flammpunkt (°C)
43.89 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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The Synthesis of Methyl Cyclopropylacetate by Palladium (II) Acetate Catalysed Reaction Of Diazomethane with Vinyl Group.
Basnak I, et al.
Synthetic Communications, 22(5), 773-782 (1992)
Jonathan D Rosen et al.
Tetrahedron letters, 50(7), 785-789 (2010-02-18)
An optimized total synthesis of the 2-amino-6-chloro-4-cyclopropyl-7-fluoro-5-methoxy-pyrido[1,2-c]pyrimidine-1,3-dione core structure of a new fluoroquinolone-like class of antibacterial agents is described. This synthesis is highlighted by a nearly quantitative ring-closing reaction to form the pyrido[1,2-c]pyrimidine core. This bicyclic ring system serves as
Charles E Mowbray et al.
Journal of medicinal chemistry, 58(24), 9615-9624 (2015-11-17)
Visceral leishmaniasis is a severe parasitic disease that is one of the most neglected tropical diseases. Treatment options are limited, and there is an urgent need for new therapeutic agents. Following an HTS campaign and hit optimization, a novel series
Phyllis A Leber et al.
Molecules (Basel, Switzerland), 19(2), 1527-1543 (2014-01-30)
The title compound 1-exo (with minor amounts of its C8 epimer 1-endo) was prepared by Wolff-Kishner reduction of the cycloadduct of 1,3-cyclohexadiene and cyclopropylketene. The [1,3]-migration product 2-endo was synthesized by efficient selective cyclopropanation of endo-5-vinylbicyclo[2.2.2]oct-2-ene at the exocyclic π-bond.
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