Weight | 67.091 g/mol |
---|---|
Formula | C4H5N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
3-BUTENENITRILE (109-75-1)
allyl cyanide · allylnitrile
Score:
#1710 in Physics
,
#4219 in Biology
,
#5316 in Chemistry
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- Syntheses, properties, and structures of anhydrous tetramethylammonium fluoride and its 1:1 adduct with trans-3-amino-2-butenenitrile (Journal of the American Chemical Society, 1990)
- Kinetics, Thermodynamics, and Effect of BPh3 on Competitive C-C and C-H Bond Activation Reactions in the Interconversion of Allyl Cyanide by (Ni(dippe)) (Journal of the American Chemical Society, 2004)
- Synthesis and Application of a New Bisphosphite Ligand Collection for Asymmetric Hydroformylation of Allyl Cyanide (Journal of Organic Chemistry, 2004)
- Direct Catalytic Asymmetric Addition of Allyl Cyanide to Ketones (Journal of the American Chemical Society, 2008)
- Transformation of the Glucosinolate-Derived Allelochemicals Allyl Isothiocyanate and Allylnitrile in Soil (Journal of Agricultural and Food Chemistry, 1995)
- Direct Catalytic Asymmetric Addition of Allyl Cyanide to Ketones via Soft Lewis Acid/Hard Brnsted Base/Hard Lewis Base Catalysis (Journal of the American Chemical Society, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - allyl cyanide
- allylnitrile
-
SMILESC=CCC#N
-
InChIKeySJNALLRHIVGIBI-UHFFFAOYSA-N
- Pubchem - 3-BUTENENITRILE
- Wikipedia - allyl cyanide
Allyl cyanide is an organic compound with the formula CH2CHCH2CN. Like other small alkyl nitriles, allyl cyanide is colorless and soluble in organic solvents. Allyl cyanide occurs naturally as an antifeedant and is used as a cross-linking agent in some polymers.
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