M3394
6-Methyl-2,4-heptanedione
≥98%
Synonym(s):
Isovalerylacetone, NSC 42238, NSC 42240, NSC 46469, NSC 94
About This Item
Recommended Products
Quality Level
Assay
≥98%
color
colorless to faint yellow
density
0.92 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
CC(C)CC(=O)CC(C)=O
InChI
1S/C8H14O2/c1-6(2)4-8(10)5-7(3)9/h6H,4-5H2,1-3H3
InChI key
IGMOYJSFRIASIE-UHFFFAOYSA-N
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Application
- Cyclocondensation and deacetylation of dibromo(phenylsulfonyl)propene derivatives for synthesis of disubstituted furans
- Synthesis of dual activity effectors of angiotensin II type 1 receptors and peroxisome proliferator-activated receptor-γ
- Addition reactions with 1-alkynes
- Knoevenagel condensation
- Oxidative free radical reactions with 2-amino-1,4-benzoquinones
- Mild oxidative cleavage for synthesis of carboxylic acids
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
138.2 °F - closed cup
Flash Point(C)
59 °C - closed cup
Personal Protective Equipment
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Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
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