264276-67-7

Basic information

• Product Name: 3,5-bis((tetrahydro-2H-pyran-2-yl)oxy)benzoic acid
• Synonyms: 3,5-bis((tetrahydro-2H-pyran-2-yl)oxy)benzoic acid
• CAS NO: 264276-67-7
• Molecular Weight: 322.358
• Mol File: 264276-67-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3,5-bis((tetrahydro-2H-pyran-2-yl)oxy)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-bis((tetrahydro-2H-pyran-2-yl)oxy)benzoic acid(264276-67-7)
• EPA Substance Registry System: 3,5-bis((tetrahydro-2H-pyran-2-yl)oxy)benzoic acid(264276-67-7)

Safety Data

• Hazardous Substances Data: 264276-67-7(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 4142-98-7 ethyl 3,5-dihydroxybenzoate 
• 945010-73-1 C₁₉H₂₆O₆ 

Downstream Products

• 957473-24-4 C₂₅H₃₁NO₅ 
• 957473-26-6 C₂₇H₄₀O₆ 

Relevant articles and documents

Size-regulable vesicles based on anion-π interactions

Taking tetraoxacalix[2]arene[2]triazine as a functionalization platform, a series of new amphiphilic molecules were synthesized in 18 to 53% yields by using a fragment coupling protocol. These amphiphilic molecules self-assembled into stable vesicles in a

Synthesis and structure of upper-rim 1,3-alternate tetraoxacalix[2]arene[2] triazine azacrowns and change of cavity in response to fluoride anion

(Chemical Equation Presented) The upper-rim 1,3-alternate tetraoxacalix[2]arene[2]triazine azacrowns were constructed effectively by macrocyclic condensation reaction of diamines with dichlorinated tetraoxacalix[2]arene[2]triazine intermediates that were