o-Toluenesulfonamide TCI T0280

Chemical Identity

CAS No.: 88-19-7
PubChem: CID 6924·SID 87576256
Formula: C7H9NO2S
Molecular weight: 171.22 g/mol
Purity: >98.0%(HPLC)(N)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-methylbenzenesulfonamide
SMILES: CC1=CC=CC=C1S(=O)(=O)N
InChIKey: YCMLQMDWSXFTIF-UHFFFAOYSA-N

Rp 662.550,00

~~Rp 478.800,00~~ Rp 662.550,00

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Toluenesulfonamide (o-Toluenesulfonamide) is a chemical compound widely used as a building block in organic synthesis. It is a key reagent in laboratory settings due to its ability to participate in various chemical reactions, including substitution and coupling reactions. This compound is particularly valuable for the synthesis of heterocyclic and aromatic compounds, making it an essential tool for chemists working on complex molecular structures. Its stability and controlled reactivity allow it to be a reliable component in a wide range of experimental procedures.

The chemical properties of Toluenesulfonamide make it a preferred choice for laboratory use. It exhibits good solubility in organic solvents such as ethyl acetate and dimethyl sulfoxide, which facilitates its use in diverse reaction conditions. Its reactivity towards nucleophilic and electrophilic reactions further enhances its versatility in synthetic pathways. These characteristics ensure that it remains a consistent and effective reagent across different experimental setups.

In Indonesian laboratories, Toluenesulfonamide is commonly used in organic chemistry research conducted by universities and research institutions. Its reliability and effectiveness in various synthetic reactions make it a staple in both academic and industrial research environments. It plays a crucial role in the development of new chemical compounds and the advancement of chemical science in Indonesia.

Related TCI products

Organic synthesis applications benefit from Toluenesulfonamide's ability to participate in substitution and coupling reactions, making it ideal for creating complex molecular structures.
It is widely used in the synthesis of heterocyclic compounds due to its reactivity and compatibility with various reaction conditions.
The compound's solubility in organic solvents like ethyl acetate and dimethyl sulfoxide makes it suitable for reactions requiring precise solvent control.
Toluenesulfonamide supports nucleophilic and electrophilic reactions, enhancing its utility in diverse synthetic pathways.
Its stability and controlled reactivity make it a reliable reagent for both academic and industrial research in Indonesian laboratories.

Brand	TCI
CAS number	88-19-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from direct sunlight

Toluenesulfonamide should be stored in a cool, dry place away from direct sunlight to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its reactivity. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its chemical nature, it should be kept away from incompatible substances to avoid potential reactions. Proper storage ensures the compound remains effective and safe for use in various experimental procedures.

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