Sodium trifluoropropylsulfinate - ≥98% , CAS No.1263377-91-8

CAS: 1263377-91-8 Cat. No.: S486596 Peso molecular: 184.11 Número EC: 808-426-6 PubChem CID: 50998692

GRADE & PURITY ≥98%

Synonyms

1263377-91-8 | 3,3,3-Trifluoropropanesulfinicacidsodiumsalt | SODIUM 3,3,3-TRIFLUOROPROPANE-1-SULFINATE | AKOS006315577 | 3,3,3-Trifluoropropanesulfinic acid sodium salt | EN300-723431 | Sodium trifluoropropylsulfinate | BARAN TFPS-NA REAGENT | E84959 | s

Storage

Argon charged,Room temperature

Descripción general

Description

The following Baran Sulfinate is a part of a toolbox of diversification reagents, which are ideal for the late-stage functionalization of nitrogen-containing heterocycles. The regioselectivity can be effectively tuned by modification of the pH and solvent selection.Radical-Based Regioselective C–H Functionalization of Electron-Deficient Heteroarenes: Scope; Tunability; and Predictability

Specifications

Sinónimos

1263377-91-8 | 3, 3, 3-Trifluoropropanesulfinicacidsodiumsalt | SODIUM 3, 3, 3-TRIFLUOROPROPANE-1-SULFINATE | AKOS006315577 | 3, 3, 3-Trifluoropropanesulfinic acid sodium salt | EN300-723431 | Sodium trifluoropropylsulfinate | BARAN TFPS-NA REAGENT | E84959 | s

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488201470
• Sonrisas canónicas: C(CS(=O)[O-])C(F)(F)F.[Na+]
• IUPAC Name: sodium;3,3,3-trifluoropropane-1-sulfinate
• InChIKey: DVCULODZLVVYHT-UHFFFAOYSA-M
• INCHI: 1S/C3H5F3O2S.Na/c4-3(5,6)1-2-9(7)8;/h1-2H2,(H,7,8);/q;+1/p-1
• Isómeros SMILES: C(CS(=O)[O-])C(F)(F)F.[Na+]
• PubChem CID: 50998692
• Peso molecular: 184.11

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Sulfinic acids and derivatives
      • Subclass Alkanesulfinic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Sulfinic acids and derivatives
• Subclass: Alkanesulfinic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkanesulfinic acids
• Alternative Parents: Organic metal halides Organosulfur compounds Organofluorides Organic sodium salts Organic oxides Hydrocarbon derivatives Alkyl fluorides Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkanesulfinic acid - Organic metal halide - Organic alkali metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organosulfur compound - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Organic cation - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as alkanesulfinic acids. These are organosulfur compounds containing an aliphatic group attached to a sulfinic acid group (or a derivative thereof), with the general formula RSO2R' (R= alkyl, R'=H).
• 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

Propiedades químicas y físicas

• Sensibilidad: air sensitive；moisture sensitive
• Peso molecular: 184.110 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 183.978 Da
• Monoisotopic Mass: 183.978 Da
• Topological Polar Surface Area: 59.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 115.000
• 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

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