93071-75-1 | 3-(Trifluoromethoxy)benzylamine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$19.00	$13.00
5g	95%	in stock	$53.00	$37.00
25g	95%	in stock	$206.00	$145.00

Description

• Catalog Number: AB44273
• Chemical Name: 3-(Trifluoromethoxy)benzylamine
• CAS Number: 93071-75-1
• Molecular Formula: C8H8F3NO
• Molecular Weight: 191.1504
• MDL Number: MFCD00061267
• SMILES: NCc1cccc(c1)OC(F)(F)F

Computed Properties

• Complexity: 160
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 2.1

Upstream Synthesis Route

3-(Trifluoromethoxy)benzylamine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its ability to introduce the trifluoromethoxy group into organic molecules. In organic synthesis, 3-(Trifluoromethoxy)benzylamine can be employed as a nucleophilic trifluoromethylating agent, enabling the conversion of various substrates to incorporate the trifluoromethoxy functionality. This trifluoromethoxy group can impart desirable properties such as increased lipophilicity, metabolic stability, and enhanced biological activity to the resulting molecules. Additionally, the presence of the benzylamine moiety in this compound offers opportunities for further derivatization through reductive amination or cross-coupling reactions, expanding its utility in the synthesis of complex organic molecules. Furthermore, the trifluoromethoxy group's electron-withdrawing nature can influence the reactivity and selectivity of chemical transformations, making 3-(Trifluoromethoxy)benzylamine a valuable tool in modern synthetic chemistry. Its application in pharmaceutical research, materials science, and agrochemical development showcases the importance of this compound in advancing various fields of study through innovative chemical synthesis strategies.