2-Cyclohexen-1-one, 97%
2-Cyclohexen-1-one, 97%
2-Cyclohexen-1-one, 97%
Thermo Scientific Chemicals

2-Cyclohexen-1-one, 97%

CAS: 930-68-7 | C6H8O | 96.13 g/mol
数量:
25 g
100 g
500 g
製品番号(カタログ番号) A15435.22
または、製品番号A15435-22
価格(JPY)
-
数量:
100 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS930-68-7
Identification (FTIR)Conforms
FormLiquid
Refractive Index1.4855-1.4905 @ 20?C
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥96.0%
さらに表示
2-Cyclohexen-1-one is used as intermediates.

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-Cyclohexen-1-one is used as intermediates.

Solubility
Soluble in water, alcohols, benzene and acetone.

Notes
Store away from oxidizing agents and strong bases. Incompatible with reducing agents and bases.
RUO – Research Use Only

General References:

  1. Gilberto M. Villacorta; C. Pulla. Rao; Stephen J. Lippard. Synthesis and reactivity of binuclear tropocoronand and related organocopper(I) complexes. Catalytic enantioselective conjugate addition of Grignard reagents to 2-cyclohexen-1-one.J. Am. Chem. Soc.1988, 110 (10), 3175-3182.
  2. Mitsunori Hashimoto; Yutaka Eda; Yasutomo Osanai; Toshiaki Iwai; Seiichi Aoki. A novel decarboxylation of α-amino acids. A facile method of decarboxylation by the use of 2-cyclohexen-1-one as a catalyst.Chemistry Letters.1986, 15 893-896.
  3. Facile, selective 1,2-reduction occurs with Sodium borohydride, 35788, in the presence of CaCl2, to give 92% yield of 2-cyclohexen-1-ol: Chem. Lett., 1847 (1991).