64750-25-0

Basic information

• Product Name: Benzoic acid, 3-hydroxy-2-pentyl-4,6-bis(phenylmethoxy)-, phenylmethyl ester
• CAS NO: 64750-25-0
• Molecular Formula: C33H34O5
• Molecular Weight: 510.63
• Mol File: 64750-25-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-hydroxy-2-pentyl-4,6-bis(phenylmethoxy)-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-hydroxy-2-pentyl-4,6-bis(phenylmethoxy)-, phenylmethyl ester(64750-25-0)
• EPA Substance Registry System: Benzoic acid, 3-hydroxy-2-pentyl-4,6-bis(phenylmethoxy)-, phenylmethyl ester(64750-25-0)

Safety Data

• Hazardous Substances Data: 64750-25-0(Hazardous Substances Data)

Upstream product

• 491-72-5 2,4-dihydroxyl-6-pentylbenzoic acid 
• 855875-40-0 2,4-dihydroxyl-6-pentylbenzaldehyde 
• 500-66-3 Olivetol 
• 64750-24-9 benzyl 4,6-bis(benzyloxy)-3-formyl-2-pentylbenzoate 
• 121903-70-6 benzyl 2,4-bis(benzyloxy)benzoate 
• 100-39-0 benzyl bromide 
• 89-86-1 4-hydroxysalicylic acid 

Downstream Products

• 522-53-2 lobaric acid 
• 1372167-27-5 lobarin 

Relevant articles and documents

METHOD FOR SYNTHESIS OF LOBARIC ACID AND ANALOG THEREOF

The present invention can synthesize lobaric acid and four analogues thereof, which are five phenolic lichen metabolites isolated from an extract of the Antarctic lichen Stereocaulon alpinum and selectively inhibit PTP1B, by a simple, economic and efficient chemical synthesis method.

Synthesis of Further Lichen Depsides

The unambiguous total synthesis of 18 lichen depsides has been achieved by the condensation of an appropriately substituted orsellinic acid and protected phenol in the key step, followed by subsequent deprotection and/or secondary reduction.The natural oc