The Methanesulfonic acid,1,1,1-trifluoro-, silver(1+) salt (1:1), with the CAS registry number 2923-28-6 and EINECS registry number 220-882-2, has the systematic name of silver trifluoromethanesulfonate. It is a kind of light beige crystalline powder, and belongs to the following product categories: Ag (Silver) Compounds; Catalysts for Organic Synthesis; Classes of Metal Compounds; Homogeneous Catalysts; Metal Triflates; Synthetic Organic Chemistry; Transition Metal Compounds. The molecular formula of this chemical is CF₃HSO₃Ag. What's more, it is usually used in the synthesis of organics, such as the preparation of Alkyl methane sulfonate, alkylation of aromatics and so on.

The physical properties of Methanesulfonic acid,1,1,1-trifluoro-, silver(1+) salt (1:1) are as following: (1)H-Bond Donor: 0; (2)H-Bond Acceptor: 6; (3)Rotatable Bond Count: 0; (4)Exact Mass: 255.857117; (5)MonoIsotopic Mass: 255.857117; (6)Topological Polar Surface Area: 65.6; (7)Heavy Atom Count: 9; (8)Formal Charge: 0; (9)Complexity: 145; (10)Isotope Atom Count: 0; (11)Defined Atom StereoCenter Count: 0; (12)Undefined Atom StereoCenter Count: 0; (13)Defined Bond StereoCenter Count: 0; (14)Undefined Bond StereoCenter Count: 0; (15)Covalently-Bonded Unit Count: 2.

Uses of Methanesulfonic acid,1,1,1-trifluoro-, silver(1+) salt (1:1): It can react with benzoyl chloride to produce benzoyl trifluoromethanesulfonate. The reaction time is 3 hours with temperature of 20°C, and the yield is about 71%.   

You should be cautious while dealing with this chemical. It irritates eyes, respiratory system and skin. Therefore, you had better take the following instructions: Wear suitable protective clothing, and in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: C(F)(F)(F)S(=O)(=O)[O-].[Ag+]
(2)InChI: InChI=1/CHF3O3S.Ag/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1
(3)InChIKey: QRUBYZBWAOOHSV-REWHXWOFAL