Weight | 83.134 g/mol |
---|---|
Formula | C5H9N |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
n-Butyl isocyanide (2769-64-4)
butyl isocyanide · n-butylisocyanide · 1-isocyanobutane
Score:
#2044 in Physics
,
#2557 in Biochemistry
,
#6366 in Chemistry
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- Palladium-catalyzed synthesis of isocoumarins and phthalides via tert-butyl isocyanide insertion. (Journal of Organic Chemistry, 2012)
- Cyclopropanation reactions of diazoalkanes with substituted olefins in the presence and absence of nickel(0) and palladium(0) catalysts. The structure of (diazofluorene)bis(tert-butyl isocyanide)nickel(0); a complex containing a .pi.-bonded diazofluorene molecule (Journal of the American Chemical Society, 1977)
- Towards molecular diversity: dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile (Organic and Biomolecular Chemistry, 2010)
- Palladium-Catalyzed One-Pot Synthesis of Quinazolinones via tert-Butyl Isocyanide Insertion (Journal of Organic Chemistry, 2014)
- Structure of bis(tert-butyl isocyanide) (tetracyanoethylene)nickel(0), Ni((CN)2=C(CN)2)(CH3)3C-N.idn.C)2 (Journal of the American Chemical Society, 1970)
- A -bonded azo-transition metal complex. The structure of bis(tert-butyl isocyanide) (azobenzene)nickel(0) (Journal of the American Chemical Society, 1972)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - butyl isocyanide
- n-butylisocyanide
- 1-isocyanobutane
-
SMILESCCCC[N+]#[C-]
-
InChIKeyFSBLVBBRXSCOKU-UHFFFAOYSA-N
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