104307-50-8

Basic information

• Product Name: 2,4-bis(benzyloxy)-6-pentylbenzoic acid
• Synonyms: 2,4-bis(benzyloxy)-6-pentylbenzoic acid
• CAS NO: 104307-50-8
• Molecular Weight: 404.506
• Mol File: 104307-50-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,4-bis(benzyloxy)-6-pentylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-bis(benzyloxy)-6-pentylbenzoic acid(104307-50-8)
• EPA Substance Registry System: 2,4-bis(benzyloxy)-6-pentylbenzoic acid(104307-50-8)

Safety Data

• Hazardous Substances Data: 104307-50-8(Hazardous Substances Data)

Upstream product

• 855875-40-0 2,4-dihydroxyl-6-pentylbenzaldehyde 
• 500-66-3 Olivetol 
• 100-39-0 benzyl bromide 
• 38862-65-6 2,4-dihydroxy-6-n-pentylbenzoic acid ethyl ester 
• 104307-49-5 ethyl 2,4-dibenzyloxy-6-pentylbenzoate 

Downstream Products

• 104307-61-1 benzyl 2,4-di-O-benzylimbricarate 
• 641-68-9 anziaic acid 
• 491-72-5 2,4-dihydroxyl-6-pentylbenzoic acid 
• 53530-24-8 benzyl 2,4-dihydroxy-6-pentylbenzoate 
• 67121-42-0 4-O-demethylimbricaric acid 
• 64750-24-9 benzyl 4,6-bis(benzyloxy)-3-formyl-2-pentylbenzoate 

Relevant articles and documents

Total Syntheses of Lobaric Acid and Its Derivatives from the Antarctic Lichen Stereocaulon alpinum

The first total syntheses of the natural products lobaric acid (1) and its derivatives isolated from the Antarctic lichen Stereocaulon alpinum are reported in this study. Lobarin (3), with a pseudodepsidone structure, was synthesized first in 11 steps by utilizing an Ullmann aryl ether coupling reaction, and lobaric acid was synthesized in an additional three steps by a seven-membered lactonization reaction. Various derivatives were also obtained from the prepared lobaric acid, and the synthetic compounds exhibited significant PTP1B inhibitory activities.

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.