214027
1,2,3,4,5-Pentamethylcyclopentadiene
95%
Synonym(s):
1,2,3,4,5-Pentamethyl-1,3-cyclopentadiene
About This Item
Recommended Products
Quality Level
Assay
95%
refractive index
n20/D 1.474 (lit.)
bp
58 °C/13 mmHg (lit.)
density
0.87 g/mL at 25 °C (lit.)
SMILES string
CC1C(C)=C(C)C(C)=C1C
InChI
1S/C10H16/c1-6-7(2)9(4)10(5)8(6)3/h6H,1-5H3
InChI key
WQIQNKQYEUMPBM-UHFFFAOYSA-N
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General description
Application
- Growth modifier chemical, during metal organic chemical vapour deposition of iron from iron pentacarbonyl.
- Ligand in "one-pot" iridium-catalyzed transformation of alcohols to amides via the intermediacy of oximes.
- Raw material for the synthesis of [Cp*Rh(bpy)H2O]2+ (Cp* = pentamethylcyclopentadienyl, bpy = 2,2′-bipyridyl), an electron mediator in the regeneration process of NADH.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
111.2 °F - closed cup
Flash Point(C)
44 °C - closed cup
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
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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