2-Methylcyclohexanone, 98%, Thermo Scientific Chemicals
2-Methylcyclohexanone, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Methylcyclohexanone, 98%, Thermo Scientific Chemicals

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Catalog number A14741.AP
also known as A14741-AP
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504.65
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Quantity:
500 mL
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Price (USD)/ Each
504.65
Online exclusive
561.00 
Save 56.35 (10%)
Add to cart
2-Methylcyclohexanone, 98%, Thermo Scientific Chemicals
Catalog numberA14741.AP
Price (USD)/ Each
504.65
Online exclusive
561.00 
Save 56.35 (10%)
-
Add to cart
Chemical Identifiers
CAS583-60-8
IUPAC Name2-methylcyclohexan-1-one
Molecular FormulaC7H12O
InChI KeyLFSAPCRASZRSKS-UHFFFAOYNA-N
SMILESCC1CCCCC1=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
Refractive Index1.4460-1.4500 @ 20?C
Identification (FTIR)Conforms
FormLiquid
Assay (GC)≥97.5%
2-Methylcyclohexanone is used as a fragrant and flavoring agent. It can also be used for the preparation of a novel pladienolide analog scaffold. Also used as a solvent.

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-Methylcyclohexanone is used as a fragrant and flavoring agent. It can also be used for the preparation of a novel pladienolide analog scaffold. Also used as a solvent.

Solubility
Insoluble in water. Soluble in methanol and diethyl ether.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Ahmed Atlamsani; Jean Marie Bregeault; Mahfoud Ziyad. Oxidation of 2-methylcyclohexanone and cyclohexanone by dioxygen catalyzed by vanadium-containing heteropolyanions. J. Org. Chem. 1993, 58, (21),5663-5665
  2. Ivan Jabin; Gilbert Revial; Alain Tomas; Pascale Lemoine; Michel Pfau. Diastereoselectivity and enantioselectivity in the addition of chiral imines of 2-methylcyclohexanone to crotonic and methacrylic acid esters. Tetrahedron: Asymmetry. 1995, 6, (7),1795-1812
  3. For use in the asymmetric synthesis of a steroid building block, see: Org. Synth. Coll., 9, 610 (1998); for reaction scheme. see (S)-(-)-1-Phenyl ethyl amine, A12632.