• 2,3-Dimethyl-1,3-benzothiazol-3-ium Iodide (CAS 2785-06-0) - TCI D6175 - AMI Scientific
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TCI

CAS 2785-06-0

2,3-Dimethyl-1,3-benzothiazol-3-ium Iodide TCI D6175

2,3-Dimethyl-1,3-benzothiazol-3-ium Iodide TCI D6175

Chemical Identity

Other names
2,3-Dimethylbenzothiazolium Iodide · 2,3-Dimethylbenzo[d]thiazol-3-ium Iodide
CAS No.
2785-06-0
PubChem
CID 459121
Formula
C9H10INS
Molecular weight
291.15 g/mol
Purity
>98.0%(HPLC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2,3-dimethyl-1,3-benzothiazol-3-ium iodide
SMILES
CC1=[N+](C2=CC=CC=C2S1)C.[I-]
InChIKey
VZRIFNLQJXPRJI-UHFFFAOYSA-M
MDL
MDL00031760
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2,3-Dimethyl-1,3-benzothiazol-3-ium Iodide is a chemical compound widely used in laboratory experiments and analytical processes. This compound plays a crucial role in organic chemistry, particularly in synthetic reactions and structural analysis. Its unique molecular structure, combining a benzothiazol ring with an iodide ion, makes it a versatile reagent in various chemical transformations. It is commonly found in research settings where complex molecular structures and high reactivity are required.

The compound is valued for its solubility in organic solvents such as ethyl acetate and ethanol, which facilitates its use in purification and reaction processes. Its chemical stability ensures consistent performance in laboratory conditions, making it reliable for repeated use. Additionally, its reactivity allows it to function as both a reactant and a catalyst in different chemical reactions. These properties make it a preferred choice for researchers seeking efficient and effective chemical tools.

In Indonesian laboratories, this compound is frequently used in organic chemistry research and analytical studies. Its availability and reactivity make it a go-to material for scientists working on complex synthesis and reaction mechanisms. It is particularly useful in applications requiring precise chemical interactions and structural modifications. Its role in both academic and industrial research underscores its importance in the chemical sciences.

Advantages (TCI brochure)

  • Acceptor unit for the terminal structure of cyanine dyes
  • Enables dyes with absorption and fluorescence in NIR and SWIR regions
  • Absorption/emission wavelengths and solubility adjustable by structure

TCI brochures (PDF)

Related TCI products

  • Organic synthesis reactions benefit from this compound's reactivity and structural versatility, enabling the creation of complex molecules.
  • Analytical chemistry uses it for its solubility and stability, aiding in the accurate detection and quantification of compounds.
  • Catalytic processes in chemical reactions are enhanced by its ability to facilitate electron transfer and substitution reactions.
  • Structural modification studies rely on its unique molecular framework to explore new chemical pathways and functional groups.
  • Research in pharmaceutical development utilizes its reactivity to design and test new drug compounds and derivatives.

From the TCI brochure

  • Synthesis of cyanine dyes
  • Biomolecular staining and bio-imaging

Brand TCI
CAS number 2785-06-0
Molecular formula —
Purity —
Category TCI
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, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances, and ensure proper ventilation when working with it. Regular monitoring of storage conditions is advised to maintain its effectiveness and safety in laboratory use.

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