Weight | 119.949 g/mol |
---|---|
Formula | C2H2BrN |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
BROMOACETONITRILE (590-17-0)
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- Catalytic effect of laser ablated Ni nanoparticles in the oxidative addition reaction for a coupling reagent of benzylchloride and bromoacetonitrile (Journal of Molecular Catalysis A-chemical, 2005)
- Unexpected formation of a spiro acridine and fused ring system from the reaction between an N-acridinylmethyl-substituted thiourea and bromoacetonitrile under basic conditions. (Journal of Organic Chemistry, 2001)
- Nickel-Catalyzed Synthesis of Arylacetonitriles from Arylzinc Chlorides and Bromoacetonitrile (Synthesis, 1987)
- Kinetics and mechanism of aquation reactions of dihalo-, diacetonitrile- and bromoacetonitrile-(3,3',3-triaminotripropylamine)cobalt(III) perchlorate (Polyhedron, 1989)
- Synthesis of -Hydroxy Nitriles via Indium-Induced Coupling of Bromoacetonitrile with Carbonyl Compounds (Bulletin of the Chemical Society of Japan, 1994)
- Iodoacetonitrile and Bromoacetonitrile as Alkylating Reagents for the Nitrogen-Phosphorus Detector (Analytical Chemistry, 1995)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C#N)Br
-
InChIKeyREXUYBKPWIPONM-UHFFFAOYSA-N
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