68119-98-2

Usage

Uses

Used in Organic Synthesis:
(3,4-Dibromo-Phenyl)-Methanol is used as a building block in the synthesis of various organic compounds, providing a convenient pathway to incorporate the 3,4-dibromophenyl group into target molecules.
Used in Chemical Reactions:
(3,4-Dibromo-Phenyl)-Methanol is used as a reagent to introduce a 3,4-dibromophenyl group into organic molecules, facilitating the formation of desired products in chemical reactions.
Used in Pharmaceutical Industry:
(3,4-Dibromo-Phenyl)-Methanol is used as an intermediate in the synthesis of biologically active compounds, contributing to the development of new pharmaceuticals with potential therapeutic applications.
Used in Research and Development:
(3,4-Dibromo-Phenyl)-Methanol is utilized in research and development settings to explore its chemical properties and potential applications, further expanding its use in various industries.

Upstream product

• 619-03-4 3,4-dibromobenzoic acid 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 51329-16-9 3,4-dibromobenzoic acid methyl ester 

Downstream Products

• 64382-93-0 1,2-dibromo-4-(bromomethyl)benzene 
• 249647-27-6 3,4-dibromophenylacetonitrile 
• 1027907-85-2 (S)-1-[3-(3,4-Dibromo-benzyl)-[1,2,4]oxadiazol-5-yl]-ethylamine 
• 1418150-40-9 C₇H₅Br₂N₃ 
• 74003-55-7 3,4-dibromobenzaldehyde 

Relevant academic research and scientific papers

Discovery of potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70

A series of 1,2,4-oxadiazole analogues has been shown to be potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70, a potential therapeutic target for immune suppression. These compounds typically are 200- 400-fold more potent than the native,

Soluble Substituted μ-Oxo(phthalocyaninato)iron(III) Dimers

Attempts to prepare various peripheral tetra- and octasubstituted (phthalocyaninato)iron derivatives RnPcFe by starting from the corresponding substituted phthalonitriles led to substituted (μ-oxo)bis compounds 2O.The tert-butyl- and ethyl-substituted systems 2O (6c) and 2O (6d) were reinvestigated.UV/Vis, FD mass, Moessbauer, NMR as well as ESR spectroscopy was used to characterize the complexes 2O to furnish evidence for the presence of Fe-O-Fe moieties in 2O.The UV/Vis data reported for 2O as well as their spectral behavior in pyridine correspond to unsubstituted 2O.Moessbauer spectra of 2O show that the complexes were obatined as a mixtures of two isomeric μ-oxo compounds A (δFe = 0.22 mm s-1, ΔEQ = 1.33-1.39 mm s-1) and B (δFe = 0.33-0.36 mm s-1, ΔEQ = 0.39-0.53 mm s-1), whose Moessbauer parameters are comparable to 2O μ-oxo(2) and μ-oxo(1), respectively.Moessbauer spectral data of 2O indicate high-spin (S = 5/2) FeIII centers.NMR-spectra of 2O (n = 4: R = tBu, Et, O(2-Et-n-C6H13), OCH2C(CH3)2CH2Ph; n = 8: R = O-n-C8H17, O(2-Et-n-C6H13) give further evidence for μ-oxo bridge structures. - Key Words: μ-Oxobis(phthalocyaninato)iron/ μ-Oxo dimers/ Moessbauer spectroscopy/ Iron complexes/ Phthalocyanines