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2-Cyclohexen-1-one, 97%, Thermo Scientific Chemicals
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Catalog number A15435.36
also known as A15435-36
Price (USD)/ Each
480.65
Online exclusive
534.00 Save 53.35 (10%)
-
Quantity:
500 g
Price (USD)/ Each
480.65
Online exclusive
534.00 Save 53.35 (10%)
2-Cyclohexen-1-one, 97%, Thermo Scientific Chemicals
Catalog numberA15435.36
Price (USD)/ Each
480.65
Online exclusive
534.00 Save 53.35 (10%)
-
Chemical Identifiers
CAS930-68-7
Specifications
Specification Sheet
Specification SheetIdentification (FTIR)Conforms
FormLiquid
Refractive Index1.4855-1.4905 @ 20?C
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥96.0%
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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.
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:
- 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.
- 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.
- 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).