34946-82-2 | Copper(ii) trifluoromethanesulfonate

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$6.00	$4.00
5g	98%	in stock	$6.00	$5.00
10g	98%	in stock	$9.00	$7.00
25g	98%	in stock	$15.00	$11.00
100g	98%	in stock	$50.00	$35.00

Description

• Catalog Number: AB45776
• Chemical Name: Copper(ii) trifluoromethanesulfonate
• CAS Number: 34946-82-2
• Molecular Formula: C2CuF6O6S2
• Molecular Weight: 361.6842
• MDL Number: MFCD00077492
• SMILES: FC(S(=O)(=O)[O-])(F)F.FC(S(=O)(=O)[O-])(F)F.[Cu+2]

Computed Properties

• Complexity: 145
• Covalently-Bonded Unit Count: 3
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 12

Upstream Synthesis Route

Copper(II) trifluoromethanesulfonate, also known as Cu(OTf)2, is a versatile reagent commonly employed in organic synthesis. Its unique properties make it a valuable solution for a variety of chemical reactions. In chemical synthesis, Cu(OTf)2 is frequently utilized as a catalyst in various transformations due to its ability to activate substrates and facilitate bond formation. This compound is particularly effective in promoting carbon-carbon and carbon-heteroatom bond formations, making it a valuable tool in the preparation of complex organic molecules. Additionally, Cu(OTf)2 is known for its high reactivity under mild reaction conditions, which allows for precise control over reaction outcomes. Its use in coupling reactions, cyclizations, and other transformations showcases its versatility and importance in modern synthetic chemistry.

Literature

• Alpha-amidation of cyclic ethers catalyzed by simple copper salt and a mild and efficient preparation method for alpha,omega-amino alcohols.

  Organic letters 20070607

• A substrate-unspecified glycosylation reaction promoted by copper(II) trifluoromethanesulfonate in benzotrifluoride.

  Carbohydrate research 20020402