1123215-07-5

Basic information

• Product Name: methyl 3,5-bis(benzyloxy)-4-hydroxybenzoate
• Synonyms: methyl 3,5-bis(benzyloxy)-4-hydroxybenzoate
• CAS NO: 1123215-07-5
• Molecular Weight: 364.398
• Mol File: 1123215-07-5.mol

Chemical Properties

• CAS DataBase Reference: methyl 3,5-bis(benzyloxy)-4-hydroxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3,5-bis(benzyloxy)-4-hydroxybenzoate(1123215-07-5)
• EPA Substance Registry System: methyl 3,5-bis(benzyloxy)-4-hydroxybenzoate(1123215-07-5)

Safety Data

• Hazardous Substances Data: 1123215-07-5(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 309758-34-7 Methyl-3,5-dibenzyl-4-allyl-gallat 
• 21022-88-8 methyl 3,5-dihydroxy-4-allyloxy benzoate 
• 99-24-1 methyl galloate 

Downstream Products

• 1357284-41-3 C₂₈H₁₉F₅O₅ 
• 70424-94-1 methyl 3,4,5-tris(benzyloxy)benzoate 
• 97152-19-7 dimethyl 4,4',5,5',6,6'-hexakis(benzyloxy)-[1,1'-biphenyl]-2,2'-dicarboxylate 
• 1404362-65-7 3,5-dihydroxy 4-(2-keto-2-anilinoethoxy)benzoic acid methyl ester 
• 1404362-64-6 methyl 3,5-bis(benzyloxy)-4-(2-oxo-2-(phenylamino)ethoxy)benzoate 
• 1404362-66-8 C₂₄H₁₉Cl₂N₇O₈ 
• 1357284-37-7 C₁₄H₇F₅O₅ 
• 1357284-46-8 C₂₂H₁₁Cl₂F₅N₆O₇ 
• 1357284-47-9 C₃₄H₁₉Cl₂F₅N₆O₅ 
• 1372789-10-0 C₄₂H₄₆O₇Si 

Relevant articles and documents

Preparation of isodehydrodigallic acid using Ullmann condensation

Isodehydrodigallic acid, which is an important component of several ellagitannin compounds, was easily synthesized using a classical Ullmann condensation reaction.

Synthesis and structure of oxacalix[2]arene[2]triazines of an expanded π-electron-deficient cavity and their interactions with anions

Novel macrocyclic anion receptors based on the principle of anion-π interactions were reported. By means of both post-macrocyclization modification protocol and the stepwise fragment coupling approach, functionalized oxacalix[2]arene[2]triazines bearing two other electron-deficient (hetero)aromatic rings on the lower rim were efficiently synthesized. The resulting oxacalix[2]arene[2]triazine macrocyclesadopt 1,3-alternate conformation, yielding therefore an expanded electron-deficient cavity or space consisting of two triazine rings and two appending aromatic rings. Spectroscopic titration study showed the selective interaction of the pentafluorophenyl- substituted oxacalix[2]arene[2]triazine with azide and fluoride in solution with the binding constants (K1:1) ranging from 1.33 × 10 3 to 3.52 × 103 M-1.