125292-98-0

Basic information

• Product Name: (R)-(-)-Agrimol B
• Synonyms: (R)-(-)-Agrimol B;(R)-1-[3,5-Bis[[2,6-dihydroxy-4-methoxy-3-methyl-5-(1-oxobutyl)phenyl]methyl]-2,4,6-trihydroxyphenyl]-2-methyl-1-butanone
• CAS NO: 125292-98-0
• Molecular Formula: C₃₇H₄₆O₁₂
• Molecular Weight: 682.75
• Mol File: 125292-98-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-(-)-Agrimol B(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(-)-Agrimol B(125292-98-0)
• EPA Substance Registry System: (R)-(-)-Agrimol B(125292-98-0)

Safety Data

• Hazardous Substances Data: 125292-98-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(R)-(-)-Agrimol B is used as a therapeutic agent for its anti-inflammatory properties, helping in the treatment of various inflammatory conditions. Its antioxidant effects also contribute to its potential use in this application.
Used in Oncology:
(R)-(-)-Agrimol B is used as a cytotoxic agent for its potential application in cancer treatment. Its significant pharmacological properties make it a promising candidate for the development of novel pharmaceutical drugs targeting cancer cells.
Used in Drug Development:
(R)-(-)-Agrimol B is used as a lead compound in the development of new pharmaceutical drugs due to its diverse biological activities and potential therapeutic applications in treating inflammatory conditions and cancer.

Upstream product

• 88-03-9 2,4,6-trihydroxytoluene 
• 1509-06-4 1-[3-methyl-2,4,6-trihydroxyphenyl]-1-butanone 
• 108-73-6 3,5-dihydroxyphenol 
• 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 
• 487-70-7 2,4,6-trihydroxybenzaldehyde 
• 6099-90-7 1,3,5-Trihydroxybenzene dihydrate 

Relevant articles and documents

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.