1049730-91-7 | 2-Bromo-4-methoxy-1-(trifluoromethoxy)benzene

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$53.00	$38.00
5g	98%	in stock	$264.00	$185.00
10g	98%	in stock	$527.00	$369.00
25g	98%	in stock	$997.00	$698.00

Description

• Catalog Number: AD47100
• Chemical Name: 2-Bromo-4-methoxy-1-(trifluoromethoxy)benzene
• CAS Number: 1049730-91-7
• Molecular Formula: C8H6BrF3O2
• Molecular Weight: 271.0312
• MDL Number: MFCD20485915
• SMILES: COc1ccc(c(c1)Br)OC(F)(F)F

Computed Properties

• Complexity: 186
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• XLogP3: 3.8

Upstream Synthesis Route

2-Bromo-4-methoxy-1-(trifluoromethoxy)benzene, also known as $name$, is a versatile compound commonly used in chemical synthesis for its unique reactivity and functional group capabilities. This compound serves as a key building block in the synthesis of various organic molecules and pharmaceuticals due to its ability to undergo multiple types of reactions.One of the primary applications of 2-Bromo-4-methoxy-1-(trifluoromethoxy)benzene in chemical synthesis is its use as a valuable starting material for the introduction of a trifluoromethoxy group into organic molecules. The trifluoromethoxy group is a highly electron-withdrawing and sterically bulky moiety that imparts valuable properties to the target molecules, such as improved bioavailability and increased metabolic stability. Additionally, the presence of the bromo and methoxy groups in 2-Bromo-4-methoxy-1-(trifluoromethoxy)benzene provides further synthetic versatility, allowing for the incorporation of additional functional groups or structural modifications.By utilizing 2-Bromo-4-methoxy-1-(trifluoromethoxy)benzene in chemical synthesis, researchers and chemists can access a wide range of synthetic pathways to develop novel compounds with diverse applications in medicinal chemistry, materials science, and agrochemicals. Its strategic placement of functional groups and reactivity make it a valuable tool for the construction of complex molecular architectures and the development of potential drug candidates.