83996-28-5

Basic information

• Product Name: Benzothiazolium, 2-methyl-3-(phenylmethyl)-, bromide
• Synonyms: 3-Benzyl-2-methyl-benzothiazolium,Bromid;2-methyl-3-benzylbenzothiazole,bromide;3-benzyl-2-methyl-benzothiazolium bromide
• CAS NO: 83996-28-5
• Molecular Formula: C15H14NS.Br
• Molecular Weight: 320.253
• Mol File: 83996-28-5.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: Benzothiazolium, 2-methyl-3-(phenylmethyl)-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazolium, 2-methyl-3-(phenylmethyl)-, bromide(83996-28-5)
• EPA Substance Registry System: Benzothiazolium, 2-methyl-3-(phenylmethyl)-, bromide(83996-28-5)

Safety Data

• Hazardous Substances Data: 83996-28-5(Hazardous Substances Data)

Upstream product

• 120-75-2 2-Methylbenzothiazole 
• 100-39-0 benzyl bromide 
• 100-46-9 benzylamine 

Downstream Products

• 83996-34-3 3-(1-acetylacetonyl)-9-benzyl-2,3a-diphenyl-3a,9-dihydrocyclopenta<1,4>benzothiazine 
• 83996-36-5 2-(1-acetylacetonyl)-9-benzyl-1,3-diphenyl-3a,9-dihydrocyclopenta<1,4>benzothiazine 
• 83996-30-9 benzothiazoline-2-spiro-6'-cyclopentafuran 
• 35746-01-1 3-benzyl-2-methylenebenzothiazoline 
• 151080-24-9 N-benzyl-2-acetylmethylidene-2,3-dihydro-1,3-benzothiazole 
• 136427-78-6 3-benzyl-2-(diformylmethylene)benzothiazoline 

Relevant articles and documents

Novel synthetic approach to near-infrared heptamethine cyanine dyes and spectroscopic characterization in presence of biological molecules

Two near-infrared symmetric heptamethine cyanine dyes, containing integrated chlorosubstituted cyclohexenyl ring were obtained via a novel synthetic approach, using mild conditions at room temperature. UV-vis and fluorescence properties of the dyes were e

Synthesis and spectral properties of near-infrared cyanine dyes showing enhanced Stokes shift: A paradigm of ICT dipolar state polymethine chromophoric systems

Three benzothiazole-derived heptamethine cyanine dyes were prepared via nucleophilic substitution at meso-position along the polymethine backbone. The synthetic route to the title polymethines includes a total of four steps starting from inexpensive comme

Solid-State Emissive Aroyl-S,N-Ketene Acetals with Tunable Aggregation-Induced Emission Characteristics

N-Benzyl aroyl-S,N-ketene acetals can be readily synthesized by condensation of aroyl chlorides and N-benzyl 2-methyl benzothiazolium salts in good to excellent yields, yielding a library of 35 chromophores with bright solid-state emission and aggregation

N-alkylated linear heptamethine polyenes as potent non-azole leads against Candida albicans fungal infections

In this study, eighteen heptamethine dyes were synthesised and their antifungal activities were evaluated against three clinically relevant yeast species. The eighteen dyes were placed within classes based on their core subunit i.e. 2,3,3-trimethylindolenine (5a-f), 1,1,2-trimethyl-1H-benzo[e]indole (6a-f), or 2-methylbenzothiazole (7a-f). The results presented herein imply that the three families of cyanine dyes, in particular compounds 5a-f, show high potential as selective scaffolds to treat C. albicans infections. This opens up the opportunity for further optimisation and investigation of this class compounds for potential antifungal treatment.