641-68-9

Basic information

• Product Name: 6-Hydroxy-4-[(2,4-dihydroxy-6-pentylbenzoyl)oxy]-2-pentylbenzoic acid
• Synonyms: 2,4-Dihydroxy-6-pentylbenzoic acid 4-carboxy-3-hydroxy-5-pentylphenyl ester;4-(2,4-Dihydroxy-6-pentylbenzoyloxy)-6-pentylsalicylic acid;6-Hydroxy-4-[(2,4-dihydroxy-6-pentylbenzoyl)oxy]-2-pentylbenzoic acid;Anziaic acid
• CAS NO: 641-68-9
• Molecular Formula: C₂₄H₃₀O₇
• Molecular Weight: 430.49
• Mol File: 641-68-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: 124 °C
• Boiling Point: 625.8±55.0 °C(Predicted)
• Appearance: /
• Density: 1.246±0.06 g/cm3(Predicted)
• PKA: 2.76±0.34(Predicted)
• CAS DataBase Reference: 6-Hydroxy-4-[(2,4-dihydroxy-6-pentylbenzoyl)oxy]-2-pentylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Hydroxy-4-[(2,4-dihydroxy-6-pentylbenzoyl)oxy]-2-pentylbenzoic acid(641-68-9)
• EPA Substance Registry System: 6-Hydroxy-4-[(2,4-dihydroxy-6-pentylbenzoyl)oxy]-2-pentylbenzoic acid(641-68-9)

Safety Data

• Hazardous Substances Data: 641-68-9(Hazardous Substances Data)

Upstream product

• 104307-50-8 2,4-bis(benzyloxy)-6-pentylbenzoic acid 
• 855875-40-0 2,4-dihydroxyl-6-pentylbenzaldehyde 
• 500-66-3 Olivetol 
• 53530-24-8 benzyl 2,4-dihydroxy-6-pentylbenzoate 
• 491-72-5 2,4-dihydroxyl-6-pentylbenzoic acid 

Downstream Products

• 106839-85-4 2,4-dihydroxy-6-pentyl-benzoic acid isopropyl ester 
• 491-72-5 2,4-dihydroxyl-6-pentylbenzoic acid 
• 38862-65-6 2,4-dihydroxy-6-n-pentylbenzoic acid ethyl ester 
• 58016-28-7 methyl 2,6-dihydroxy-6-pentylbenzoate 
• 64185-31-5 Anziasaeuremethylester 
• 5366-08-5 Planasaeuremethylester 

Relevant articles and documents

Synthesis and antibacterial evaluation of anziaic acid and its analogues as topoisomerase i inhibitors

Naturally occurring anziaic acid has very recently been reported as a topoisomerase I inhibitor with antibacterial activity. Herein total synthesis of anziaic acid and its structural analogues is described and the preliminary structure-activity relationship (SAR) has been developed based on topoisomerase inhibition and whole cell antibacterial activity.