| Weight | 271.936 g/mol |
|---|---|
| Formula | C6H8Br2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
2,3-DIBROMOPROPYL ACRYLATE (19660-16-3)
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LabBot
- Terpolymerization of acrylonitrile, styrene, and 2,3dibromopropyl acrylate (Journal of Polymer Science Part A, 1983)
- Thermal degradation of bromine-containing polymers. Part 7Poly(2,3-dibromopropyl methacrylate) and poly(2,3-dibromopropyl acrylate) (Polymer Degradation and Stability, 1986)
- Thermal degradation of bromine-containing polymers: Part 10Copolymers of 2,3-dibromopropyl methacrylate and 2,3-dibromopropyl acrylate with methyl acrylate (Polymer Degradation and Stability, 1987)
- Polyester / Cotton poly -2,3- dibromopropyl acrylate ( PDBPA ) (1977)
- Copolymerization of Acrylonitrile and 2,3-dibromopropyl acrylate system (1978)
- Thermal degradation of bromine-containing polymers: Part 11Blends of poly(2,3-dibromopropyl methacrylate) and poly(2,3-dibromopropyl acrylate) with poly(methyl methacrylate) and poly(methyl acrylate) (Polymer Degradation and Stability, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=CC(=O)OCC(CBr)Br
-
InChIKeyMUKJDVAYJDKPAG-UHFFFAOYSA-N
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Most-cited Publications
Safety
Trends
Alternate Names
External Links
Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Reactant
+
N-Bromosuccinimide
(Wohl-Ziegler reaction)
Reactant
+
CARBON TETRACHLORIDE
(Appel reaction)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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(29921-57-1)
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(371-49-3)
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(36847-51-5)
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3-METHOXYBUTYL ACETATE
(4435-53-4)
1 alternate name
3 suppliers
2,3-DIBROMOPROPYL ACRYLATE
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