I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
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
Highly flammable liquid and vapour.
Precautionary Statements: P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378q-P501c
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Keep container tightly closed. Ground/bond container and receiving equipment. Use explosion-proof electrical/ventilating/lighting/ equipment. Use only non-sparking tools. Take precautionary measures against static discharge. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. In case of fire: Use CO2, dry chemical, or foam Dispose of contents/ container to an approved waste disposal plant