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63141-08-2

Ethanone, 1-(1-bromocyclopropyl)- (9CI)

Catalog#: AR00EINH  |   CAS#: 63141-08-2  |   MDL#: MFCD18976261  |   MF: C5H7BrO  |   MW: 163.0125

Packsize Purity Price Availability Quantity
50mg 95% $393.00 2-3 weeks Buy Now Add To Cart
100mg 95% $571.00 2-3 weeks Buy Now Add To Cart
250mg 95% $805.00 2-3 weeks Buy Now Add To Cart
500mg 95% $1,252.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,598.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $3,330.00 2-3 weeks Buy Now Add To Cart
5g 95% $6,557.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00EINH
Chemical Name Ethanone, 1-(1-bromocyclopropyl)- (9CI)
CAS Number 63141-08-2
Molecular Formula C5H7BrO
Molecular Weight 163.0125
MDL Number MFCD18976261
SMILES CC(=O)C1(Br)CC1

1-(1-Bromocyclopropyl)ethanone, also known as bromocyclopropyl ketone, is a valuable reagent in chemical synthesis due to its unique structure and reactivity. This compound serves as a versatile building block in organic chemistry, particularly in the synthesis of complex molecules and pharmaceuticals.One of the key applications of 1-(1-Bromocyclopropyl)ethanone is its use as a precursor in the preparation of substituted cyclopropyl ketones. By undergoing various chemical transformations, such as nucleophilic substitution or cross-coupling reactions, this compound can be converted into a wide range of functionalized cyclopropyl ketones. These derivatives are important intermediates in the synthesis of biologically active compounds and natural products.Additionally, 1-(1-Bromocyclopropyl)ethanone can participate in cyclopropanation reactions, where it acts as a cyclopropyl carbene precursor. This reactivity enables the formation of strained cyclopropane rings in organic molecules, which can significantly impact their chemical and biological properties.In summary, the application of 1-(1-Bromocyclopropyl)ethanone in chemical synthesis offers synthetic chemists a powerful tool for accessing structurally diverse and biologically relevant compounds through controlled reactivity and strategic functional group manipulations.
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