497959-33-8 | 2-Bromo-4-(trifluoromethyl)benzyl alcohol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$26.00	$18.00
5g	95%	in stock	$28.00	$20.00
10g	95%	in stock	$55.00	$39.00
25g	95%	in stock	$120.00	$84.00

Description

• Catalog Number: AG17630
• Chemical Name: 2-Bromo-4-(trifluoromethyl)benzyl alcohol
• CAS Number: 497959-33-8
• Molecular Formula: C8H6BrF3O
• Molecular Weight: 255.0318
• MDL Number: MFCD03788534
• SMILES: OCc1ccc(cc1Br)C(F)(F)F

Computed Properties

• Complexity: 171
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.6

Upstream Synthesis Route

In chemical synthesis, 2-Bromo-4-(trifluoromethyl)benzyl alcohol serves as a valuable building block for creating a diverse range of organic compounds. This versatile compound is commonly utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure, characterized by the presence of a bromine atom and a trifluoromethyl group on a benzyl alcohol moiety, imparts specific reactivity and functional properties that are crucial for facilitating various synthetic transformations.One of the primary applications of 2-Bromo-4-(trifluoromethyl)benzyl alcohol is in the preparation of complex organic molecules through nucleophilic substitution reactions. By leveraging the reactivity of the bromine atom, chemists can introduce this functional group into target molecules with precision, enabling the synthesis of novel pharmaceutical agents or bioactive compounds. Additionally, the trifluoromethyl group serves as a valuable synthetic handle for further elaboration, allowing for the introduction of additional functionality or the modification of physicochemical properties.Furthermore, 2-Bromo-4-(trifluoromethyl)benzyl alcohol can participate in diverse synthetic pathways, including metal-catalyzed cross-coupling reactions, radical reactions, and organometallic transformations. Its compatibility with a wide range of synthetic methodologies makes it a versatile building block for accessing structurally complex and diverse chemical scaffolds. In the realm of medicinal chemistry, this compound's ability to modulate molecular properties and enhance biological activity makes it a valuable tool for drug discovery and development.Overall, the strategic incorporation of 2-Bromo-4-(trifluoromethyl)benzyl alcohol in chemical synthesis enables researchers to access a myriad of functionalized molecules with potential applications in various industries, highlighting its significance as a key component in modern organic synthesis strategies.