129536-40-9

Basic information

• Product Name: Benzenemethanol, 3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]-
• CAS NO: 129536-40-9
• Molecular Formula: C49H44O7
• Molecular Weight: 744.884
• Mol File: 129536-40-9.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]-(129536-40-9)
• EPA Substance Registry System: Benzenemethanol, 3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]-(129536-40-9)

Safety Data

• Hazardous Substances Data: 129536-40-9(Hazardous Substances Data)

Usage

General Description

Benzenemethanol, 3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]-, also known as bisphenol A (BPA), is a chemical compound commonly used in the production of plastics and epoxy resins. It is a colorless solid with a faint, sweet odor, and is used in a variety of consumer products such as food and drink containers, thermal paper receipts, and dental sealants. However, concerns have been raised about the potential health effects of BPA, as it can leach from products and be ingested or absorbed by the body. Research has linked BPA exposure to hormone disruption, reproductive issues, and an increased risk of certain health conditions such as obesity, diabetes, and cancer. As a result, many countries have implemented regulations and restrictions on the use of BPA in certain products.

Upstream product

• 58605-10-0 methyl 3,5-bis(benzyloxy)benzoate 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 24131-32-6 3,5-bis(benzyloxy)benzyl bromide 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 67093-27-0 3,5-dibenzyloxybenzyl chloride 
• 194083-69-7 C₅₁H₄₆O₈ 
• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 80457-61-0 methanesulfonyl 3,5-dibenzyloxybenzyl alcohol 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 137472-18-5 3,5-bis(3,5-bis(benzyloxy)benzyloxy)benzaldehyde 
• 137472-14-1 methyl 3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy] benzoate 

Downstream Products

• 184219-30-5 C₄₉H₄₃ClO₆ 
• 246512-25-4 methanesulfonic acid 3,5-bis-(3,5-bis-benzyloxy-benzyloxy)-benzyl ester 
• 129536-41-0 3,5-bis[3,5-bis(benzyloxy)benzyloxy]benzyl bromide 
• 943297-62-9 C₅₉H₅₇BrO₁₂ 
• 496839-77-1 9-({3,5-bis[3,5-bis(benzyloxy)benzyloxy]benzyloxy}methyl)anthracene 
• 137472-18-5 3,5-bis(3,5-bis(benzyloxy)benzyloxy)benzaldehyde 
• 207562-27-4 4-(3',5'-Di(3'',5''dibenzyloxy)benzyloxy)benzyloxyphthalonitrile 
• 1160525-56-3 C₅₉H₅₂O₁₁ 
• 1345133-82-5 C₈₆H₈₈N₂O₁₄Si 
• 811473-56-0 [G-2]-N₃ 
• 1206798-35-7 C₆₄H₆₄N₂O₉ 

Relevant articles and documents

Hydrogen-bonded dendronized polymers and their self-assembly in solution

Frechet-type benzyl ether dendrons of second and third generations with a carboxyl group (G2, G3) at the apex site could attach to poly(4-vinylpyridine) (PVP), forming hydrogen-bonded dendronized polymers (HB denpols) in their common solvent, chloroform. The HB denpols show unique self-assembly behavior, forming vesicles in the common solvent under ultrasonic treatment. The structure and morphology of the vesicles were characterized by dynamic light scattering (DLS), static light scattering (SLS), SEM, TEM, and AFM. The size of the vesicles decreases and the thickness of the vascular membrane increases as the molar ratio of Gx/PVP increases. The hydrogen bonding. π-π aromatic stacking of the dendrons. and the considerable difference in architecture between the dendron Gx and PVP are the main factors facilitating the assembly of the HB denpols in the common solvent.

Dendrimer solid acid and polymer electrolyte membrane including the same

Provided are a dendrimer solid acid and a polymer electrolyte membrane using the same. The polymer electrolyte membrane includes a macromolecule of a dendrimer solid acid having ionically conductive terminal groups at the surface thereof and a minimum amo

Synthesis of organometallic poly(dendrimer)s by macromonomer polymerization: effect of dendrimer size and structural rigidity on the polymerization efficiency

Two series of first to third generation (G1-G3) oligoether dendrimers, one hearing a shorter spacer chain (C-O) and the other having a longer spacer branch (C-C-C-O) were prepared. Both series of compounds, containing two reactive C≡CH moieties on the dendrimer surface, were used as macromonomers and copolymerized with trans-[Pt(PEt3)2Cl2] to form organometallic poly(dendrimer)s by an outer-sphere-outer-sphere connection strategy. It was found that concentration of monomer used in the polymerization, the dendrimer generation, and, most strikingly, the length of the spacer were key factors that determined the polymerization efficiency. Hence, the structurally more rigid and compact C-O linked dendrimers formed poly(dendrimer)s with a higher degree of polymerization than the structurally less rigid and more bulky C-C-C-O dendrimers. This result was due to the higher tendency to form cyclic oligomers in the latter series of compounds. In addition, the differences in the polymerization efficiency among the three generations of dendrimers could be explained by the gradual decrease of reactive functional group density on the dendrimer surface.

Triazole-linked dendro[60]fullerenes: modular synthesis via a 'click' reaction and acidity-dependent self-assembly on the surface

A series of Fréchet-type dendron functionalized [60]fullerene derivatives that bear a 1,2,3-triazole linkage group, referred to as triazole-linked dendro[60]fullerenes, were prepared via a modular synthetic protocol based on a Cu-catalyzed [3+2] cycloaddi