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Thermo Scientific Chemicals
2-Methylcyclohexane-1,3-dione, 98+%
CAS: 1193-55-1 | C7H10O2 | 126.16 g/mol
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CAS1193-55-1
規格
規格表
規格表Assay (HPLC)≥98.0%
Identification (FTIR)Conforms
Loss on Drying≤3% (105°C/constant weight)
Appearance (Color)White to cream to pale yellow
FormCrystals or powder or crystalline powder
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2-Methylcyclohexane-1,3-dione acts as a synthetic intermediate. It is an important starting material, exemplified in a formal synthesis of acorone. It is also used in Organic Synthesis, Pharmaceuticals, Agrochemicals.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Methylcyclohexane-1,3-dione acts as a synthetic intermediate. It is an important starting material, exemplified in a formal synthesis of acorone. It is also used in Organic Synthesis, Pharmaceuticals, Agrochemicals.
Solubility
Soluble in methanol ( 0.1 g/mL). Insoluble in water.
Notes
Hygroscopic. Store at -20°C. Incompatible with oxidizing agents and moisture.
2-Methylcyclohexane-1,3-dione acts as a synthetic intermediate. It is an important starting material, exemplified in a formal synthesis of acorone. It is also used in Organic Synthesis, Pharmaceuticals, Agrochemicals.
Solubility
Soluble in methanol ( 0.1 g/mL). Insoluble in water.
Notes
Hygroscopic. Store at -20°C. Incompatible with oxidizing agents and moisture.
RUO – Research Use Only
General References:
- Tetsuji Yanami; Michiharu Kato; Masaaki Miyashita; Akira Yoshikoshi, Yasuhiro Itagaki; Kenji Matsuura. Oxygen transfer reaction in acetonylation of 2-methylcyclohexane-1,3-dione with 2-nitropropene. J. Org. Chem. 1977, 42, (16), 2779-2781.
- Useful building block for ring B of the steroid nucleus: J. Am. Chem. Soc., 79, 5542 (1957); J. Chem. Soc., 3441 (1957); Helv. Chim. Acta, 36, 482 (1953). For C-methylation using MeI and Benzyl trimethyl ammonium hydroxide, A14927, see: Org. Synth. Coll., 8, 312 (1993).