63992-61-0

Usage

InChI:InChI=1/C7H6Cl2O2/c1-3-6(8)4(10)2-5(11)7(3)9/h2,10-11H,1H3

Upstream product

• 428-21-7 Geodoxin 
• 3405-51-4 (+/-)-Erdin 
• 7664-93-9 sulfuric acid 
• 11029-16-6 2-(3,5-dichloro-2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoic acid 
• 28917-43-3 3,5-dibenzyloxybenzoic acid 
• 2151-16-8 methyl 2-(3,5-dichloro-2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoate 
• 80457-61-0 methanesulfonyl 3,5-dibenzyloxybenzyl alcohol 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 36776-43-9 (((5-methyl-1,3-phenylene)bis(oxy))bis(methylene))dibenzene 
• 737800-17-8 1,5-Bis-benzyloxy-2,4-dichloro-3-methyl-benzene 
• 73855-53-5 3,5-dichloro-2,6-dihydroxy-4-methyl-benzoic acid 

Downstream Products

• 153478-14-9 2,4-dichloro-1,5-dimethoxy-3-methylbenzene 
• 261958-57-0 2-bromo-4,6-dichloro-5-methylbenzene-1,3-diol 
• 2151-16-8 methyl 2-(3,5-dichloro-2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoate 
• 261958-61-6 2-[2,6-bis(methoxymethoxy)-3,5-dichloro-4-methylbenzoyl]-3-methoxy-5-(methoxymethoxy)benzaldehyde 
• 261958-60-5 2-[2,6-bis(methoxymethoxy)-3,5-dichloro-4-methylbenzoyl]-3-methoxy-5-(methoxymethoxy)benzyl alcohol 
• 261958-62-7 2-(3,5-dichloro-2,6-bis-methoxymethoxy-4-methyl-benzoyl)-3-methoxy-5-methoxymethoxy-benzoic acid 
• 261958-63-8 methyl 2-[2,6-bis(methoxymethoxy)-3,5-dichloro-4-methylbenzoyl]-3-methoxy-5-(methoxymethoxy)benzoate 
• 261958-59-2 2'-benzyloxymethyl-6'-methoxy-2,4',6-tris(methoxymethoxy)-3,5-dichloro-4-methylbenzophenone 
• 261958-58-1 4-{[2-benzyloxymethyl-6-methoxy-4-(methoxymethoxy)phenyl]hydroxymethyl}-3,5-bis(methoxymethoxy)-2,6-dichlorotoluene 
• 261958-52-5 3,5-bis(methoxymethoxy)-4-bromo-2,6-dichlorotoluene 

Relevant academic research and scientific papers

The first total synthesis of SB87-Cl and pestalone, novel bioactive benzophenone natural products

SB87-Cl 1, an inhibitor of testosterone-5α-reductase, and pestalone 2 exhibiting effective antimicrobial activity against MRSA (MIC=37ng/mL) and VRE (MIC=78ng/mL), were novel bioactive benzophenone natural products. Total synthesis of 1 and 2 has been successfully accomplished. The common synthetic precursor 18 of 1 and 2, was successfully obtained by the coupling of 8 with 12.