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2,3-Dimethyl-1,3-butadiene undergoes Diels Alder cycloaddition reaction and it also participates in polymerization reactions. It is also involved in manufacturing of synthetic rubber.
For examples of use in Diels-Alder reactions, see: Org. Synth. Coll., 3, 310 (1955); 7, 4 (1990). For an asymmetric Diels-Alder reaction catalyzed by a chiral acyloxyborane, see: Org. Synth. Coll., 9, 722 (1998).
For use in phosphole synthesis, see Dichlorophenylphosphine, A10284./n
Uemura, T.; Nakanishi, R.; Mochizuki, S.; Murata,Y.; Kitagawa, S. Radical polymerization of 2,3-dimethyl-1,3-butadiene in coordination nanochannels. Chem. Commun. 2015, 51 (48), 9892-9895.
Nakashim, E.; Yamamoto, H. Continuous flow of nitroso Diels-Alder reaction. Chem. Commun. 2015, 51 (61), 12309-12312.
Hazard Statements: H225-H304
Highly flammable liquid and vapour. May be fatal if swallowed and enters airways.
Precautionary Statements: P210-P280a-P301+P310a-P303+P361+P353-P405-P501a
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Wear protective gloves and eye/face protection. IF SWALLOWED: Immediately call a POISON CENTER/doctor IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.