Isobutyl Methanesulfonate - ≥98%(GC) , CAS No.16156-53-9

CAS: 16156-53-9 Cat. No.: I305089 Formule: C₅H₁₂O₃S Poids moléculaire: 152.21 Numéro CE: 812-808-8

GRADE & PURITY ≥98%(GC)

Synonyms

SCHEMBL776575 | METHANESULFONIC ACID, ISOBUTYL ESTER | X7Y6L6AB2M | METHANESULPHONIC ACID, ISOBUTYL ESTER | PZMKMCFRTKGVOL-UHFFFAOYSA-N | ISOBUTYL METHANESULPHONATE | EN300-383257 | Methanesulfonic acid, 2-methylpropyl ester | Isobutyl methanesulfonate |

Storage

Room temperature,Desiccated

Shipped In

Normal

Specifications

Synonymes

SCHEMBL776575 | METHANESULFONIC ACID, ISOBUTYL ESTER | X7Y6L6AB2M | METHANESULPHONIC ACID, ISOBUTYL ESTER | PZMKMCFRTKGVOL-UHFFFAOYSA-N | ISOBUTYL METHANESULPHONATE | EN300-383257 | Methanesulfonic acid, 2-methylpropyl ester | Isobutyl methanesulfonate |

Spécifications et pureté

≥98%(GC)

Conditions de stockage de stockage

Room temperature,Desiccated

Expédié en

Normal

Pureté

≥98%(GC)

Noms et identifiants

• Pubchem Sid: 504756812
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756812
• Sourires canoniques: CC(C)COS(=O)(=O)C
• IUPAC Name: 2-methylpropyl methanesulfonate
• InChIKey: PZMKMCFRTKGVOL-UHFFFAOYSA-N
• INCHI: 1S/C5H12O3S/c1-5(2)4-8-9(3,6)7/h5H,4H2,1-3H3
• Isomères SMILES: CC(C)COS(=O)(=O)C
• Poids moléculaire: 152.21
• Reaxy-Rn: 1753435
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1753435&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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 Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organosulfonic acid ester - Sulfonic acid ester - Sulfonyl - Methanesulfonate - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Aliphatic acyclic compound
• Description: 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

Propriétés chimiques et physiques

• Indice de réfraction: 1.43
• Point d'éclair (°C): 97 °C
• Point d'ébullition (°C): 53°C|1mmHg(lit.)
• Poids moléculaire: 152.210 g/mol
• XLogP3: 1.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 152.051 Da
• Monoisotopic Mass: 152.051 Da
• Topological Polar Surface Area: 51.800 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 152.000
• 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