Silver trifluoromethanesulfonate - ≥97% , CAS No.2923-28-6

CAS: 2923-28-6 Cat. No.: S106655 Molecular Weight: 256.94 Beilstein Registry Number: 3598402 EC Number: 220-882-2 PubChem CID: 76223

GRADE & PURITY ≥97%

Synonyms

Methanesulfonic acid, 1,1,1-trifluoro-, silver(1+) salt (1:1) | N-propan-2-ylcyclohexanamine | Silver trifluoromethanesulfonate, purum, >=98.0% (Ag) | Silver(I) trifluoromethanesulfonate | DTXSID5062716 | Silver trifluoromethanesulfonate, >=99% | silver(1

Storage

Protected from light,Room temperature,Argon charged,Desiccated,Cool

Shipped In

Normal

Specifications

Synonyms

Methanesulfonic acid, 1, 1, 1-trifluoro-, silver(1+) salt (1:1) | N-propan-2-ylcyclohexanamine | Silver trifluoromethanesulfonate, purum, >=98.0% (Ag) | Silver(I) trifluoromethanesulfonate | DTXSID5062716 | Silver trifluoromethanesulfonate, >=99% | silver(1

Specifications & Purity

≥97%

Storage

Protected from light, Room temperature, Argon charged, Desiccated, Cool

Shipped In

Normal

Purity

≥97%

Names and Identifiers

• Canonical Smiles: C(F)(F)(F)S(=O)(=O)[O-].[Ag+]
• IUPAC Name: silver;trifluoromethanesulfonate
• InChIKey: QRUBYZBWAOOHSV-UHFFFAOYSA-M
• INCHI: 1S/CHF3O3S.Ag/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1
• Isomeric SMILES: C(F)(F)(F)S(=O)(=O)[O-].[Ag+]
• WGK Germany: 3
• PubChem CID: 76223
• Molecular Weight: 256.94
• Beilstein: 3598402
• Reaxy-Rn: 3598402

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Organic sulfonic acids and derivatives
      • Subclass Organosulfonic acids and derivatives
        • Level5 Alkanesulfonic acids and derivatives
          • Level6 Alkanesulfonic acids
            • Level7 Trifluoromethanesulfonates

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Organic sulfonic acids and derivatives
• Subclass: Organosulfonic acids and derivatives
• Intermediate Tree Nodes: Alkanesulfonic acids and derivatives - Alkanesulfonic acids
• Direct Parent: Trifluoromethanesulfonates
• Alternative Parents: Sulfonyls Organosulfonic acids Methanesulfonates Trihalomethanes Organic metal halides Organofluorides Organic silver salts Organic oxides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trifluoromethanesulfonate - Methanesulfonate - Organosulfonic acid - Sulfonyl - Trihalomethane - Organic metal halide - Organic transition metal salt - Alkyl fluoride - Organic silver salt - Hydrocarbon derivative - Organic salt - Halomethane - Organic oxide - Organosulfur compound - Organofluoride - Organohalogen compound - Organic oxygen compound - Alkyl halide - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as trifluoromethanesulfonates. These are alkanesulfonic acids, that contain a sulfonate group that is substituted with a trifluoromethyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in water
• Sensitivity: Hygroscopic.light & air sensitive
• Melt Point(°C): 356°C
• Molecular Weight: 256.940 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 255.857 Da
• Monoisotopic Mass: 255.857 Da
• Topological Polar Surface Area: 65.600 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 145.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

References

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