16492-75-4

Usage

Uses

Used in Pharmaceutical Synthesis:
1,2,3-Benzenetriol, 5-bromois used as an intermediate in the synthesis of pharmaceuticals for its unique properties and reactivity. The presence of the bromine group allows for further functionalization and modification of the molecule, making it a versatile building block in the development of new drugs.
Used in Dye Synthesis:
1,2,3-Benzenetriol, 5-bromois used as a precursor in the synthesis of dyes due to its ability to form colored compounds. The bromine atoms in the molecule can be replaced with other functional groups, leading to the formation of various dyes with different colors and properties.
Used in Organic Compounds Synthesis:
1,2,3-Benzenetriol, 5-bromois used as a starting material in the synthesis of other organic compounds. Its reactivity and the presence of the bromine group make it suitable for various organic reactions, such as substitution, addition, and coupling reactions, to produce a wide range of organic compounds.
Used in Antioxidant Applications:
1,2,3-Benzenetriol, 5-bromois used as an antioxidant due to its ability to scavenge free radicals and protect cells from oxidative damage. Its antioxidant properties have been studied for potential use in the treatment of diseases associated with oxidative stress, such as cancer and diabetes.
Used in Cancer Treatment Research:
1,2,3-Benzenetriol, 5-bromohas been studied for its potential use in the treatment of cancer due to its ability to modulate various signaling pathways involved in tumor growth and progression. Further research is needed to explore its efficacy and safety as a cancer therapeutic agent.

Upstream product

• 17345-74-3 4,5,6-tribromo-pyrogallol 
• 2675-79-8 1-bromo-3,4,5-trimethoxybenzene 
• 70654-71-6 4-bromo-2,6-dimethoxyphenol 
• 133932-61-3 5-bromo-2-methoxybenzene-1,3-diol 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 

Downstream Products

• 695816-76-3 5-bromo-1,2,3-tris(decyloxy)benzene 
• 695816-77-4 3,4,5-tri((3S)-3,7-dimethyl-1-octyloxy)bromobenzene 
• 654065-52-8 1-bromo-3,4,5-tris-n-dodecyloxybenzene 
• 875753-80-3 C₃₃H₅₉BrO₁₅ 
• 875753-81-4 C₃₈H₆₈O₁₅Si 
• 437762-53-3 3,4,5-tridodecyloxyphenylacetylene 
• 654065-53-9 3,4,5-tris(n-dodecan-1-yloxy)-1-(2-trimethylsilyl)ethynylbenzene 
• 2675-79-8 1-bromo-3,4,5-trimethoxybenzene 
• 1041859-46-4 5-bromo-1,2,3-tris(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene 
• 1092504-79-4 C₉₀H₇₇BrO₁₂ 
• 1143294-00-1 C₂₇H₂₃BrO₃ 
• 1135950-13-8 (R,R,R)-5-bromo-1,2,3-tris-(2-[2-(2-(2-[2-(2-methoxyethoxy)ethoxy]ethoxy)ethoxy)ethoxy]ethoxy-2-propoxy)benzene 
• 1135950-12-7 5-bromo-1,2,3-tris-(2-[2-(2-(2-[2-(2-methoxyethoxy)ethoxy]ethoxy)ethoxy)ethoxy]ethoxy)benzene 
• 1239569-10-8 5-bromo-1,2,3-triicosyloxybenzene 

Relevant academic research and scientific papers

Membrane-Anchoring Photosensitizer with Aggregation-Induced Emission Characteristics for Combating Multidrug-Resistant Bacteria

Traditional photosensitizers (PSs) show reduced singlet oxygen (1O2) production and quenched fluorescence upon aggregation in aqueous media, which greatly affect their efficiency in photodynamic therapy (PDT). Meanwhile, non-targetin

Synthesis and helical supramolecular organization of discotic liquid crystalline dibenzo[: Hi, st] ovalene

Dibenzo[hi,st]ovalene (DBOV) has emerged as a new polycyclic aromatic hydrocarbon (PAH) with intriguing optical properties with strong red emission. Nevertheless, DBOV derivatives thus far synthesized either had mesityl groups that hinder the π-π stacking

Synthesis and Liquid Crystalline Self-Assembly of Concave Diindoles with a Hydropentalene Core

Fischer indole reaction of Weiss diketone with 4-bromophenylhydrazine provided the 2,8-dibromo-hexahydropentaleno[2,1-b:5,4-b’]diindole key intermediate, which was converted to the target compounds by N-protection/Suzuki cross-coupling. Variation of prote

Thermotropic columnar liquid crystals based on wedge-shaped phenylphosphonic acids

Wedge-shaped phenylphosphonic acids with variation in the peripheral alkoxy chains have been synthesized. These derivatives show a hexagonal columnar liquid-crystalline behavior upon thermal treatment. These materials have potential to be used as efficien

A Membrane-Intercalating Conjugated Oligoelectrolyte with High-Efficiency Photodynamic Antimicrobial Activity

A membrane-intercalating conjugated oligoelectrolyte (COE), PTTP, was designed and synthesized with the goal of providing red-shifted absorption spectra relative to previously synthesized COE analogs. Specifically, electron-rich and electron-poor subunits were introduced in the conjugated backbone to modulate the band gap. PTTP exhibits maxima of absorption at 507 nm and of emission at 725 nm. PTTP can also efficiently function to generate singlet oxygen in situ (ΦΔ≈20 %) and has appropriate topology and dimensions to interact with lipid membranes. The resulting rapid membrane insertion and sensitizing ability provide PTTP with a highly efficient antibacterial capability under a low light dose (0.6 J cm?2) toward Gram-negative bacteria E. coli, making it a remarkably efficient optically mediated antimicrobial agent.

Tetradentate platinum(II) complexes: Synthesis, photophysical properties, liquid crystalline characteristics and charge transport behaviour

Three new tetradentate phosphorescent Pt(II) complexes (Pt6, Pt12 and Pt16) with half-disc molecule structure were designed and synthesized, which are based on tetradentate ligands with six alkoxyl chains on the periphery,

A columnar liquid crystal with permanent polar order

The self-assembly of axial dipolar subphthalocyanine molecules in the presence of electric fields leads to uniaxially oriented columnar liquid crystalline materials that exhibit permanent polarization.

Partially stripped insulated nanowires: A lightly substituted hexa-peri-hexabenzocoronene-based columnar liquid crystal

We present the facile preparation and characterization of the first "unwrapped" hexa-peri-hexabenzocoronene derivative, which forms a stable columnar liquid crystalline mesophase with a practically accessible isotropization temperature.

Efficient preparation of stereopure amphiphilic 1,2-amino alcohols by using preparative enantioselective HPLC

Chiral amphiphiles are useful for controlling the structures and properties of supramolecular assemblies, but their stereocontrolled synthesis is generally difficult, because their long alkyl chains tend to bring unfavorable effects on the solubility, rea

The liquid crystal Click procedure for oligothiophene-Tethered phthalocyanines-self-Assembly, alignment and photocurrent

A series of star-shaped liquid crystals (LCs) with a phthalocyanine donor core, oligothiophene antennae and fullerene acceptors have been successfully prepared. This hierarchical self-Assembly results in a nanosegregated helical donor-Acceptor-Antennae LC-system promoted by the recently discovered Click procedure. This model system reveals all photophysical prerequisites for energy conversion, charge generation and transport. Uniform amorphous thin films of 150 nm could be produced by bar-coating. Annealing did not only induce the formation of columns via the Click procedure but also partially homeotropically aligned the non-clearing sample in a sandwich geometry (ITO and Ag/MoO3). This has been confirmed by microscopic studies and the measurement of photocurrent, which increased by a factor of 300 after the annealing step.