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69383-59-1

1-Bromo-2,4-dimethyl-5-nitrobenzene

Catalog#: AR005NIV  |   CAS#: 69383-59-1  |   MDL#: MFCD00075824  |   MF: C8H8BrNO2  |   MW: 230.0586

Packsize Purity Price Availability Quantity
1g 98% $4.00 Global Stock Buy Now Add To Cart
5g 98% $8.00 Global Stock Buy Now Add To Cart
10g 98% $14.00 Global Stock Buy Now Add To Cart
25g 98% $32.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005NIV
Chemical Name 1-Bromo-2,4-dimethyl-5-nitrobenzene
CAS Number 69383-59-1
Molecular Formula C8H8BrNO2
Molecular Weight 230.0586
MDL Number MFCD00075824
SMILES [O-][N+](=O)c1cc(Br)c(cc1C)C

1-Bromo-2,4-dimethyl-5-nitrobenzene, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis processes. This compound plays a crucial role in the development of various organic compounds through its unique reactivity and functional groups. In particular, $name$ is frequently employed as a key intermediate in the synthesis of complex pharmaceuticals, agrochemicals, and specialty chemicals.One of the primary applications of 1-Bromo-2,4-dimethyl-5-nitrobenzene in chemical synthesis is as a starting material for the construction of biologically active molecules. Its nitro and bromo functional groups provide valuable synthetic handles for further elaboration, allowing chemists to introduce a wide range of substituents and structural modifications. This flexibility makes $name$ an essential building block for the creation of diverse chemical structures with specific properties and functions.Moreover, the unique structural features of 1-Bromo-2,4-dimethyl-5-nitrobenzene make it a valuable reagent in the field of organic synthesis. Its electron-withdrawing nitro group and bulky methyl substituents influence the regioselectivity and stereoselectivity of reactions, leading to the formation of target molecules with high efficiency and selectivity. Chemists leverage these characteristics to control the course of various transformations, such as nucleophilic substitution, cross-coupling reactions, and aromatic functionalization.Overall, the strategic use of 1-Bromo-2,4-dimethyl-5-nitrobenzene in chemical synthesis enables researchers to access structurally diverse compounds with enhanced biological activities, improved pharmacokinetic properties, and tailored functionalities. By harnessing the synthetic potential of this versatile compound, chemists can expedite the development of novel materials and therapeutic agents that address current challenges in the fields of medicine, agriculture, and materials science.
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