536164
0.97 (vs air)
35.04 atm ( 20 °C)
99.99%
842 °F
36 %
−104 °C (lit.)
−169 °C (lit.)
C=C
1S/C2H4/c1-2/h1-2H2
VGGSQFUCUMXWEO-UHFFFAOYSA-N
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Danger
Flam. Gas 1 - Press. Gas Liquefied gas - STOT SE 3
Central nervous system
2A - Gases
nwg
-148.0 °F - closed cup
-100 °C - closed cup
dust mask type N95 (US), Eyeshields, Gloves
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The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. Since the reaction involves the formation of a cyclic product via a cyclic transition state, it is also referred to as a "cycloaddition".
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