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CAS 4209-18-1

3-Benzyl-4-methylthiazolium Chloride TCI B1940

3-Benzyl-4-methylthiazolium Chloride TCI B1940

Chemical Identity

CAS No.
4209-18-1
PubChem
CID 12324835·SID 87564824
Formula
C11H12ClNS
Molecular weight
225.74 g/mol
Purity
>98.0%(HPLC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3-benzyl-4-methyl-1,3-thiazol-3-ium chloride
SMILES
CC1=CSC=[N+]1CC2=CC=CC=C2.[Cl-]
InChIKey
ZGBNEPNQIDHABT-UHFFFAOYSA-M
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3-Benzyl-4-methylthiazolium Chloride is a chemical compound widely used in organic chemistry reactions within laboratory settings. As a heterocyclic building block, it serves as a versatile intermediate in the synthesis of complex molecules. Its unique structure allows it to participate in various chemical transformations, including substitution, reduction, and coupling reactions. This compound is particularly valuable in the development of new synthetic pathways due to its reactivity and structural adaptability.

The compound exhibits chemical stability under controlled conditions, making it a reliable reagent for laboratory applications. However, it is sensitive to moisture and light, which necessitates careful handling and storage. These properties make it an ideal choice for reactions requiring precise environmental control. Its ability to form compounds with specific biological activities further enhances its utility in pharmaceutical and biochemical research.

In Indonesian laboratories, 3-Benzyl-4-methylthiazolium Chloride is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds. Its availability and high quality make it a preferred material for researchers seeking to explore complex molecular structures and reactivity. The compound plays a key role in advancing chemical synthesis and drug development efforts in the region.

  • Heterocyclic Compound Synthesis: This compound is ideal for creating complex ring structures, making it essential in pharmaceutical research.
  • Organic Reaction Substitution: Its reactivity allows it to participate in substitution reactions, enhancing the diversity of synthetic pathways.
  • Bioactive Molecule Development: The compound's ability to form biologically active molecules makes it valuable in drug discovery and development.
  • Environmental Controlled Reactions: Its sensitivity to moisture and light makes it suitable for reactions requiring precise environmental conditions.
  • Structural Complexity Exploration: Researchers use it to study and manipulate complex molecular architectures in synthetic chemistry.

Brand TCI
CAS number 4209-18-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid powder
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment to prevent degradation due to moisture and light exposure. It is recommended to use airtight containers to maintain its chemical stability. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its sensitivity, it should be kept away from sources of heat and direct sunlight. Proper labeling and storage conditions are essential to ensure the compound remains effective for its intended applications. Regular inspection of storage conditions is advised to maintain the integrity of the material.

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