5453-04-3

Basic information

• Product Name: Gossypol acetic acid
• Synonyms: GOSSYPOL, ACETATE (SALT);2,3,8-trihydroxy-6-methyl-4-propan-2-yl-7-(1,6,7-trihydroxy-8-methanoyl-3-methyl-5-propan-2-yl-naphthalen-2-yl)naphthalene-1-carbaldehyde;7-(8-formyl-1,6,7-trihydroxy-3-methyl-5-propan-2-ylnaphthalen-2-yl)-2,3,8-trihydroxy-6-methyl-4-propan-2-ylnaphthalene-1-carbaldehyde;7-(8-formyl-1,6,7-trihydroxy-5-isopropyl-3-methyl-2-naphthyl)-2,3,8-trihydroxy-4-isopropyl-6-methyl-naphthalene-1-carbaldehyde
• CAS NO: 5453-04-3
• Molecular Formula: C₂H₄O₂*C₃₀H₃₀O₈
• Molecular Weight: 578.61
• Mol File: 5453-04-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Gossypol acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: Gossypol acetic acid(5453-04-3)
• EPA Substance Registry System: Gossypol acetic acid(5453-04-3)

Safety Data

• Hazardous Substances Data: 5453-04-3(Hazardous Substances Data)

Upstream product

• 303-45-7 (rac)-gossypol 
• 64-19-7 acetic acid 

Downstream Products

• 784206-41-3 apogossypol 
• 109046-69-7 1,6,7,1',6',7'-hexahydroxy-5,5'-diisopropyl-3,3'-dimethyl-[2,2']binaphthyl-8,8'-dicarbaldehyde bis-(4-acetyl-phenylimine) 
• 109968-47-0 1,6,7,1',6',7'-hexahydroxy-5,5'-diisopropyl-3,3'-dimethyl-[2,2']binaphthyl-8,8'-dicarbaldehyde bis-benzylimine 
• 125185-20-8 dianilinegossypol 
• 119264-73-2 1,6,1',6'-Tetrahydroxy-8,8'-bis-[1-(4-hydroxy-phenylamino)-meth-(Z)-ylidene]-5,5'-diisopropyl-3,3'-dimethyl-8H,8'H-[2,2']binaphthalenyl-7,7'-dione 

Relevant articles and documents

A gossypol derivatives and their use in inhibiting urease activity

The invention relates to the technical field of fertilizer, and particularly relates to gossypol derivatives and an application thereof in inhibition of urease activity. The gossypol derivatives have the chemical structural general formula described in the specification, wherein R represents a part except amino in amino acid, and the amino acid is amino acid containing primary amino. The gossypol derivatives take gossypol as an aldehyde group providing reagent and are prepared by modifying the aldehyde group of gossypol with the amino of the amino acid. When the gossypol derivatives are applied in preparation of urease inhibitors, the urease inhibition effect is good, and the IC50 value inhibiting soil ammonia volatilization effect is as low as 1.56*10 mol.L. Compared with a gossypol raw material, the gossypol derivatives have better solubility, are more stable and are convenient to use; and a part of gossypol derivatives have the urease inhibition activity significantly enhanced.