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7214-50-8

2-Cyclohexen-1-one, 5-methyl-

Catalog#: AR005KI5  |   CAS#: 7214-50-8  |   MDL#: MFCD02685515  |   MF: C7H10O  |   MW: 110.1537

Packsize Purity Price Availability Quantity
50mg 95% $211.00 2-3 weeks Buy Now Add To Cart
100mg 95% $303.00 2-3 weeks Buy Now Add To Cart
250mg 95% $423.00 2-3 weeks Buy Now Add To Cart
500mg 95% $685.00 2-3 weeks Buy Now Add To Cart
1g 95% $870.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR005KI5
Chemical Name 2-Cyclohexen-1-one, 5-methyl-
CAS Number 7214-50-8
Molecular Formula C7H10O
Molecular Weight 110.1537
MDL Number MFCD02685515
SMILES CC1CC(=O)C=CC1

5-Methylcyclohex-2-en-1-one, also known as 5-methyl-2-cyclohexen-1-one, serves as a versatile building block in chemical synthesis due to its unique structural features and reactivity. This compound is widely employed in organic chemistry for the creation of diverse chemical compounds and complex molecules.One key application of 5-Methylcyclohex-2-en-1-one is its use as a precursor in the synthesis of various pharmaceuticals and fine chemicals. Its cyclohexenone moiety provides a valuable platform for the introduction of new functional groups and structural modifications. By undergoing various chemical transformations such as oxidation, reduction, and functional group modifications, this compound can be utilized to generate a wide range of derivatives with different properties and applications.Furthermore, 5-Methylcyclohex-2-en-1-one plays a crucial role in the preparation of natural products and bioactive compounds. Its reactivity allows chemists to efficiently access complex molecular scaffolds found in biologically active molecules. Through strategic manipulation of its structure, researchers can design and synthesize novel compounds with potential pharmacological activities and therapeutic properties.In summary, 5-Methylcyclohex-2-en-1-one serves as a valuable synthon in chemical synthesis, enabling the construction of diverse organic molecules, pharmaceuticals, and natural products through strategic functionalization and derivatization. Its versatile nature and reactivity make it an indispensable tool for synthetic chemists seeking to access new chemical entities and explore the frontiers of organic synthesis.
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