26104-00-7

Basic information

• Product Name: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-
• CAS NO: 26104-00-7
• Molecular Formula: C11H16O3
• Molecular Weight: 196.246
• Mol File: 26104-00-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-(26104-00-7)
• EPA Substance Registry System: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-(26104-00-7)

Safety Data

• Hazardous Substances Data: 26104-00-7(Hazardous Substances Data)

Upstream product

• 26103-97-9 phloroisovalerophenone 
• 80902-65-4 2-(3-methylbuta-2-enyl)-1,3,5-trihydroxybenzene 
• 108-73-6 3,5-dihydroxyphenol 
• 541-28-6 isopentyl iodide 
• 108-12-3 isopentanoyl chloride 
• 27364-71-2 2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone 

Downstream Products

• 750643-46-0 2,4,6-trihydroxy-3-isopentyl-benzaldehyde 
• 219954-72-0 3,5-diformyl-isopentyl phloroglucinol 
• 39652-85-2 2',4',6'-trihydroxy-3'-(3-methylbutyl)acetophenone 
• 860541-06-6 [4,5-dimethoxy-2-(2,4,6-trihydroxy-3-isopentyl-phenacyl)-phenoxy]-acetic acid 
• 14764-75-1 4,6-Di-(p-toluolsulfonyloxy)-2-hydroxy-3-isopentyl-acetophenon 
• 14764-82-0 2.4.4'.6'-Tetramethoxy-2'-hydroxy-3'-isopentyl-chalkon 
• 14764-79-5 2.4.2'.4'-Tetramethoxy-6'-hydroxy-3'-isopentyl-chalkon 
• 14764-81-9 2'-hydroxy-3'-isopentyl-4',6'-dimethoxyacetophenone 
• 14764-78-4 6-Hydroxy-2,4-dimethoxy-3-isopentyl-acetophenon 
• 14764-77-3 4,6-Dibenzyloxy-2-hydroxy-3-isopentyl-acetophenon 
• 14764-76-2 4,6-Dihydroxy-2-methoxy-3-isopentyl-acetophenon 
• 115120-54-2 3-methyl-1-(2,4,6-trihydroxy-3-isopentyl-5-phenylazo-phenyl)-butan-1-one 
• 479-17-4 2,6-dihydroxy-3-isopentyl-5-isovaleryl-[1,4]benzoquinone 
• 26104-02-9 2',4',6'-Trihydroxy-3'-isopentyl-5'-isovaleryl-isovalerophenon 

Relevant articles and documents

Antiprotozoal and antimicrobial activities of O-alkylated and formylated acylphloroglucinols

In the present article, we examined the antileishmanial, antimalarial, antibacterial, and antifungal activities of several newly synthesized O-alkylated phloroglucinol compounds (11-19) which are analogues of the naturally occurring antimalarial compound