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CAS 16156-53-9

Isobutyl Methanesulfonate TCI I1062

Isobutyl Methanesulfonate TCI I1062

Chemical Identity

CAS No.
16156-53-9
PubChem
CID 119240·SID 354334896
Formula
C5H12O3S
Molecular weight
152.21 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-methylpropyl methanesulfonate
SMILES
CC(C)COS(=O)(=O)C
InChIKey
PZMKMCFRTKGVOL-UHFFFAOYSA-N
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Isobutyl Methanesulfonate (IMS) is a chemical compound widely utilized in organic synthesis reactions within laboratory settings. As a key building block, IMS plays a crucial role in facilitating various chemical transformations, particularly in substitution and nucleophilic reactions. Its structural characteristics allow it to act as an effective electrophilic reagent, making it a versatile component in synthetic pathways. IMS is commonly used as a starting material for the synthesis of complex organic molecules that require specific reactivity. Its stability under controlled conditions makes it a reliable reagent for laboratory applications.

IMS is preferred due to its consistent chemical properties and stability in laboratory environments. It exhibits good solubility in organic solvents such as ethyl acetate and ethanol, which simplifies mixing and reaction processes. The compound’s ability to function as an electron donor enhances its reactivity in polar environments, making it suitable for a range of synthetic procedures. Its predictable behavior and compatibility with various reaction conditions contribute to its popularity among chemists.

In Indonesian laboratories, IMS is extensively used in chemical research, particularly in the development of new compounds and molecular modifications. It is a common reagent in both educational and applied research settings, supporting both teaching and experimental work. Many research institutions and universities rely on IMS for its reliability and effectiveness in various chemical processes.

  • Organic synthesis reactions benefit from IMS due to its reactivity and stability, enabling efficient chemical transformations.
  • Molecular modification projects utilize IMS to create complex structures with controlled reactivity and functional groups.
  • Educational laboratories use IMS to demonstrate nucleophilic and substitution reactions, providing hands-on learning experiences.
  • Industrial research applications incorporate IMS for its consistent performance in large-scale chemical processes.
  • Analytical chemistry experiments rely on IMS for its solubility and reactivity in polar solvents, aiding in compound characterization.

Brand TCI
CAS number 16156-53-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various sizes as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

IMS should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and maintain chemical integrity. As a reactive compound, IMS should be handled with appropriate personal protective equipment, including gloves and safety goggles. It is important to ensure proper ventilation in the workspace to minimize exposure. IMS is not flammable but should be kept away from incompatible materials. Regular monitoring of storage conditions ensures the compound remains stable and suitable for laboratory use.

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