| Weight | 90.509 g/mol |
|---|---|
| Formula | C3H3ClO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Acryloyl chloride (814-68-6)
Score:
#26 in Physical chemistry
,
#119 in Materials science
,
#986 in Physics
,
#2819 in Chemistry
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- Sigma-Aldrich - Acryloyl chloride50.50 - 793.00 USD
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- Surface covalent encapsulation of multiwalled carbon nanotubes with poly(acryloyl chloride) grafted poly(ethylene glycol) (Journal of Polymer Science Part A, 2006)
- Emission spectroscopy of the predissociative excited state dynamics of acrolein, acrylic acid, and acryloyl chloride at 199 nm (Journal of Chemical Physics, 1995)
- Surface molecular tailoring via pulsed plasma-generated acryloyl chloride polymers : Synthesis and reactivity (Macromolecules, 1998)
- Microwave spectrum of s-trans acryloyl chloride (Journal of Molecular Spectroscopy, 1972)
- 1-Cyanoethanoyl-4-acryloyl thiosemicarbazide and its metal complexes as thermal stabilizers for rigid poly(vinyl chloride) (Polymer Degradation and Stability, 1999)
- Radiosynthesis of ML03, a novel positron emission tomography biomarker for targeting epidermal growth factor receptor via the labeling synthon: [11C]acryloyl chloride (Applied Radiation and Isotopes, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=CC(=O)Cl
-
InChIKeyHFBMWMNUJJDEQZ-UHFFFAOYSA-N
- Pubchem - Acryloyl chloride
- Wikipedia - Acryloyl chloride
Acryloyl chloride, also known as 2-propenoyl chloride or acrylic acid chloride, is a clear, light yellow, flammable liquid with an acrid smell. It belongs to the acid chlorides group of compounds and is therefore a derivative of acrylic acid.
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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Acryloyl chloride
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