10193-50-7

Basic information

• Product Name: 3,3'-Methylenebisphenol
• Synonyms: 3,3'-Methylenebisphenol
• CAS NO: 10193-50-7
• Molecular Formula: C₁₃H₁₂O₂
• Molecular Weight: 0
• Mol File: 10193-50-7.mol

Chemical Properties

• Melting Point: 102.5°C
• Boiling Point: 297.96°C (rough estimate)
• Appearance: /
• Density: 1.0907 (rough estimate)
• Refractive Index: 1.6110 (estimate)
• CAS DataBase Reference: 3,3'-Methylenebisphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3'-Methylenebisphenol(10193-50-7)
• EPA Substance Registry System: 3,3'-Methylenebisphenol(10193-50-7)

Safety Data

• Hazardous Substances Data: 10193-50-7(Hazardous Substances Data)

Upstream product

• 36282-40-3 (3-methoxyphenyl)magnesium bromide 
• 51095-48-8 bis(3-methoxyphenyl)methane 
• 591-31-1 3-methoxy-benzaldehyde 
• 50-00-0 formaldehyd 
• 108-95-2 phenol 
• 19471-12-6 3,3'-methylenedianiline 

Downstream Products

• 86248-27-3 4,4'-methylenebis(2-hydroxybenzaldehyde) 

Relevant articles and documents

Green synthesis of bisphenol F over 12-phosphotungstic acid supported on acid-activated palygorskite

In this study, acid-activated palygorskite (Pa) with tunable surface acidity was obtained by simple acidic treatment of raw clay. The new catalysts with 5-30 wt% 12-phosphotungstic acid (H3O40PW12·xH2O, PTA) were then readily prepared by the wet impregnation method. Their characteristic features were systematically investigated by various means including energy-dispersive X-ray (EDX), X-ray diffraction (XRD), N2 adsorption/desorption isotherms, Fourier-transform infrared spectroscopy (FT-IR), thermo-gravimetric analysis (TGA), as well by comparison with Pa, PTA and H-Beta zeolite. The high activities of these catalysts promoted phenol to undergo hydroxyalkylation, resulting in an interesting bisphenol F (BPF) product. Among these solid acid catalysts, 10% PTA/Pa was chosen as the most suitable catalyst giving an 87% yield and 96% selectivity under mild conditions (phenol/formaldehyde mole ratio of 15: 1; T = 343 K; catalyst concentration of 0.006 g g-1; 40 min). The surface acid strength and acidic type were characterized by ammonia temperature programmed desorption of NH3 (NH3-TPD), and FT-IR of pyridine adsorption (Py-IR). It was found that the catalytic activity could be further enhanced by impregnating PTA onto Pa due to the enhanced acid strength and the redistribution of Br?nsted and Lewis acid sites. Besides, a more appropriate combination of Br?nsted and Lewis acid sites was essential to achieve the highest BPF yield. Recycle experiments were conducted and a plausible mechanistic pathway was proposed according to our observations and findings.

A Bisphenolic Honokiol Analog Outcompetes Oral Antimicrobial Agent Cetylpyridinium Chloride via a Membrane-Associated Mechanism

Targeting Streptococcus mutans is the primary focus in reducing dental caries, one of the most common maladies in the world. Previously, our groups discovered a potent bactericidal biaryl compound that was inspired by the natural product honokiol. Herein, a structure activity relationship (SAR) study to ascertain structural motifs key to inhibition is outlined. Furthermore, mechanism studies show that bacterial membrane disruption is central to the bacterial growth inhibition. During this process, it was discovered that analog C2 demonstrated a 4-fold better therapeutic index compared to the commercially available antimicrobial cetylpyridinium chloride (CPC) making it a viable alternative for oral care.

Metal Arene Complexes in Organic Synthesis. Hydroxylation, Trimethylsilylation, and Carbethoxylation of Some Polycyclic Aromatic Hydrocarbons Utilizing η6-Arene-Chromium Tricarbonyl Complexes

The deprotonation of polycyclic aromatic hydrocarbon (PAH) chromium tricarbonyl complexes (PAH = naphthalene, anthracene, phenanthrene, pyrene, fluoranthene) using an in situ technique where the PAH complex, the base (LiTMP or LDA), and the electrophile (trialkyl borate, trimethylsilyl chloride, or ethyl chloroformate) were placed in solution simultaneously resulted in hydroxylation, trimethylsilylation, or carbethoxylation of the PAH after oxidative workup where the regiochemistry was controlled by steric factors.As a result, substitution at positions of the PAHs not readily available by electrophilic substitution were obtained in some cases.Conditions minimizing isomer mixtures and factors affecting the regiochemistry and the scope of the reaction sequence were examined.

Carbonates of acetylenic alcohols

Polymerizable carbonate compounds of the formula: wherein A is an aromatic polycycle, R1 and R2 are independently hydrogen atom or alkyl, and n is 1, 2 or 3, are disclosed. They are useful as a component of nonemanating, self-curing and heat resistant resin compositions.