55576-66-4

Usage

Uses

Used in Pharmaceutical Applications:
Agrimol B is used as an anti-inflammatory agent for its ability to reduce inflammation, which can be beneficial in treating various inflammatory conditions.
Agrimol B is used as an antimicrobial agent for its capacity to inhibit the growth of microorganisms, making it a potential candidate for treating bacterial infections.
Agrimol B is used as an antifungal agent for its effectiveness against fungal infections, offering a natural alternative for combating fungal pathogens.
Used in Agricultural Applications:
Agrimol B is used as a pesticide for its potential to control pests, leveraging its antimicrobial and antifungal properties to protect crops.
Agrimol B is used as a herbicide for its ability to inhibit the growth of unwanted plants, suggesting its utility in managing weed populations in agricultural settings.

InChI:InChI=1/C37H46O12/c1-9-12-23(38)25-32(44)19(29(41)17(5)36(25)48-7)14-21-31(43)22(35(47)27(34(21)46)28(40)16(4)11-3)15-20-30(42)18(6)37(49-8)26(33(20)45)24(39)13-10-2/h16,41-47H,9-15H2,1-8H3/t16-/m0/s1

Upstream product

• 6099-90-7 1,3,5-Trihydroxybenzene dihydrate 
• 487-70-7 2,4,6-trihydroxybenzaldehyde 
• 50-00-0 formaldehyd 
• 478-48-8 1-4,6-dihydroxy-2-methoxy-3-methylphenylbutan-1-one 
• 125074-06-8 2-methyl-1-(2,4,6-trihydroxyphenyl)-1-butanone 
• 108-73-6 3,5-dihydroxyphenol 
• 1509-06-4 1-[3-methyl-2,4,6-trihydroxyphenyl]-1-butanone 
• 88-03-9 2,4,6-trihydroxytoluene 

Relevant academic research and scientific papers

Synthetic method of pilosin B and intermediate pseudomonophenols thereof

The invention discloses a method for synthesizing pilosin B and intermediate pseudomonophenols thereof. The synthesis method of the pseudo-sheep equol comprises the step E. Step F and Step g. The synthetic method of the pilosin B provided by the invention is prepared by the following steps H, step J, preparation of the pseudomonophenols synthesized by the above method, and preparation of the pseudomonophenols synthesized by the method in step I. In step E, the novel amino protecting reagent with good reaction with the phenolic hydroxyl group is used as a protecting reagent, the phenol hydroxyl group of each intermediate in the intermediate molecule fragment a synthesis process is selectively protected, the reagent types are reduced and the use of toxic reagents such as benzyl chloride and the like is avoided.

Preparation method of phloroglucinol derivative and intermediate

The invention discloses a preparation method of a phloroglucinol derivative and an intermediate. The preparation method of the phloroglucinol derivative includes the step: performing reaction on a compound 1 and a compound 3 under the action of lewis acid in an aprotic organic solvent to obtain the phloroglucinol derivative. The phloroglucinol derivative is provided with an agrimophol B, the preparation method is simple, easy to operate, mild in reaction condition and high in synthetic yield, chromatographic column separation is omitted, synthetic cost is reduced, and industrial mass production is facilitated.