Propargyl Methanesulfonate Ester - ≥98% , CAS No.16156-58-4

CAS: 16156-58-4 Cat. No.: P350637 Summenformel: C₄H₆O₃S Molekulargewicht: 134.15 EG-Nummer: 808-222-7 PubChem CID: 305925

GRADE & PURITY ≥98%

Synonyms

propargyl methanesulfonate | FT-0674061 | NSC203079 | NSC-203079 | Benzenamine,2-(phenylthio)-,hydrochloride(1:1) | s11862 | propargyl mesylate | MFCD09841205 | 2-Propyn-1-ol, 1-methanesulfonate | Propargyl Methanesulfonate Ester | prop-2-ynyl methanesulf

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Übersicht

Application：

The presence of electrolyte additives enhances the performance of lithium ion batteries by improving their thermal stability and ionic conductivity. Additives also reduce the flammability of electrolytes and provide overcharge protection. 2-Propynyl methanesulfonate finds application as additive in lithium ion batteries.

Specifications

Synonyme

propargyl methanesulfonate | FT-0674061 | NSC203079 | NSC-203079 | Benzenamine,2-(phenylthio)-,hydrochloride(1:1) | s11862 | propargyl mesylate | MFCD09841205 | 2-Propyn-1-ol, 1-methanesulfonate | Propargyl Methanesulfonate Ester | prop-2-ynyl methanesulf

Spezifikationen & Reinheit

≥98%

Storage

Store at 2-8°C,Protected from light,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

504758412

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504758412

Kanonisches Lächeln

CS(=O)(=O)OCC#C

IUPAC Name

prop-2-ynyl methanesulfonate

InChIKey

OWAHJGWVERXJMI-UHFFFAOYSA-N

INCHI

1S/C4H6O3S/c1-3-4-7-8(2,5)6/h1H,4H2,2H3

Isomere SMILES

CS(=O)(=O)OCC#C

PubChem CID

305925

Molekulargewicht

134.15

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Organic sulfonic acids and derivatives
      • Subclass Organosulfonic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Organic sulfonic acids and derivatives
• Subclass: Organosulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Organosulfonic acid esters
• Alternative Parents: Sulfonic acid esters Sulfonyls Methanesulfonates Acetylides Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organosulfonic acid ester - Sulfonic acid ester - Sulfonyl - Methanesulfonate - Acetylide - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as organosulfonic acid esters. These are esters of sulfonic acid, which have the general structure RS(=O)2OR' (R,R' = organyl, not 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in Chloroform and Methanol
• Empfindlichkeit: Light sensitive；Heat sensitive；Moisture sensitive
• Molekulargewicht: 134.160 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 134.004 Da
• Monoisotopic Mass: 134.004 Da
• Topological Polar Surface Area: 51.800 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 187.000
• 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: 1