715-33-3

Usage

Uses

Used in Pharmaceutical Industry:
METHYL 3,5-DIBROMO-2,4-DIHYDROXY-6-METHYLBENZOATE is used as an intermediate in the synthesis of various drugs and pharmaceuticals, contributing to the development of new therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, METHYL 3,5-DIBROMO-2,4-DIHYDROXY-6-METHYLBENZOATE is employed as a key component in the creation of complex organic molecules, facilitating the advancement of chemical research and innovation.
Used in Antifungal Applications:
METHYL 3,5-DIBROMO-2,4-DIHYDROXY-6-METHYLBENZOATE is studied for its potential antifungal properties, indicating its possible use in combating fungal infections and contributing to the development of antifungal agents.
Used in Antibacterial Applications:
Additionally, METHYL 3,5-DIBROMO-2,4-DIHYDROXY-6-METHYLBENZOATE has been investigated for its potential antibacterial properties, suggesting its use in the development of antibacterial substances to address bacterial infections.

InChI:InChI=1/C9H8Br2O4/c1-3-4(9(14)15-2)7(12)6(11)8(13)5(3)10/h12-13H,1-2H3

Upstream product

• 3187-58-4 methyl orsellinate 
• 56157-27-8 methyl 6-methyl-2,4-cyclohexanedione-1-carboxylate 
• 39493-30-6 methyl 2-hydroxy-6-methyl-4-oxocyclohex-2-enecarboxylate 
• 39493-62-4 2-oxo-4-hydroxy-6-methyl-cyclohex-3-ene carboxylic acid methyl ester 

Downstream Products

• 150965-73-4 methyl 3,5-dibromo-2,4-dimethoxy-6-methylbenzoate 
• 3187-58-4 methyl orsellinate 
• 56526-84-2 methyl 3-bromo-4,6-dimethoxy-2-methylbenzoate 
• 157826-57-8 3-bromo-4,6-dimethoxy-2-methyl-5-(3-methyl-2-butenyl)benzyl alcohol 
• 157826-52-3 methyl 3-bromo-4,6-dimethoxy-2-methyl-5-(3-methyl-2-butenyl)benzoate 
• 157826-51-2 methyl 3-bromo-<(E)-3,7-dimethyl-2,6-octadienyl>-4,6-dimethoxy-2-methylbenzoate 

Relevant academic research and scientific papers

CANNABIDIOL-TYPE CANNABINOID COMPOUND

The present invention relates to a cannabidiol (CBD) type cannabinoid compound for use as a medicament. The CBD-type cannabinoid, cannabidiol-C1 (CBD-C1), is a naturally occurring cannabinoid that can be found in minor quantities in the cannabis plant. Furthermore, the 5 cannabinoid can be produced by synthetic means and a method for the production of CBD-C1 is described herein. In addition, disclosed herein are data which demonstrate the efficacy of CBD-C1 in models of disease.

Asymmetric synthesis and structure-activity studies of the fungal metabolites colletorin A, colletochlorin A and their halogenates analogues

The first asymmetric total synthesis of both enantiomers of the natural products colletorin A and colletochlorin A is presented. The proposed methodology is based on the coupling reaction between highly substituted aromatic Gilman cuprates and optically active allyl bromides, in turn obtained by Sharpless asymmetric dihydroxylation. The latter ensured a high degree of regio- and stereocontrol in the enantioselective step of the synthesis. The same synthetic strategy has been also applied for the preparation of differently halogenated synthetic analogues of colletochlorin A in high enantiomeric purity. The enantioselective synthesis of colletorin A and colletochlorin A allows to reliably assign their absolute configuration. Preliminary assessment of their herbicidal and insecticidal properties evidence the possibility to modulate the bioactivity of these compounds, highlighting its dependence on both the absolute stereochemistry and the halogen nature.

Cajan element structure and methods in the application of preparing antibacterial drug

The invention belongs to the field of medicines and discloses a longistyline analogue and an application thereof in preparation of an antibacterial drug. The longistyline analogue has a structure as shown in the formula I described in the specification, w

Regiodefined synthesis of brominated hydroxyanthraquinones related to proisocrinins

Dibromobenzoisofuranone 12, synthesized in six steps, was regiospecifically annulated with 5-substituted cyclohexenones 13/36 in the presence of LiOt-Bu to give brominated anthraquinones 14/38 in good yields. Darzens condensation of 30 was shown to give c