1189105-68-7 | 4-Bromo-6-(trifluoromethoxy)quinoline

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$73.00	$51.00
1g	95%	in stock	$201.00	$141.00
5g	95%	in stock	$572.00	$400.00
10g	95%	in stock	$945.00	$661.00
25g	95%	in stock	$1,878.00	$1,315.00

Description

• Catalog Number: AD33072
• Chemical Name: 4-Bromo-6-(trifluoromethoxy)quinoline
• CAS Number: 1189105-68-7
• Molecular Formula: C10H5BrF3NO
• Molecular Weight: 292.052
• MDL Number: MFCD12674963
• SMILES: Brc1ccnc2c1cc(cc2)OC(F)(F)F

Computed Properties

• Complexity: 249
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• XLogP3: 4.1

Upstream Synthesis Route

4-Bromo-6-(trifluoromethoxy)quinoline is a versatile compound frequently employed in chemical synthesis for its unique reactivity and functional group compatibility. This specialized quinoline derivative is particularly valuable in the field of organic synthesis due to its ability to undergo diverse chemical transformations, leading to the formation of intricate molecular structures and complex organic compounds. One of the prominent applications of 4-Bromo-6-(trifluoromethoxy)quinoline is in the synthesis of novel pharmaceuticals and agrochemicals. Its trifluoromethoxy group and bromine substituent can serve as key handles for further modification, allowing chemists to introduce specific functional groups or structural motifs required for enhancing biological activity or improving chemical properties. The presence of the quinoline scaffold also imparts desirable properties, such as aromaticity and electron density, which can influence the reactivity and selectivity of subsequent reactions.In addition to its role in drug discovery and agricultural chemistry, 4-Bromo-6-(trifluoromethoxy)quinoline finds applications in material science, where it can be utilized in the design and synthesis of advanced materials with tailored properties. Its unique combination of reactive sites and electron-deficient nature makes this compound an attractive building block for the construction of functional materials, polymers, and organic dyes with diverse applications ranging from electronic devices to sensors.Overall, the versatility and synthetic utility of 4-Bromo-6-(trifluoromethoxy)quinoline make it a valuable tool for chemists seeking to access complex molecular architectures and functionalized compounds for a wide range of applications in the fields of pharmaceuticals, agrochemicals, and materials science.