• 1. An approach to 7-aza-1-phosphanorbornane complexes: strain promoted rearrangement of 1-iminylphosphirane complexes and cycloaddition with olefins?
  Yang Xu,Min Wang,Donghui Wei,Rongqiang Tian,Zheng Duan,Fran?ois Mathey Dalton Trans., 2019,48, 5523-5526
• 2. An alumina stabilized graphene oxide wrapped SnO2 hollow sphere LIB anode with improved lithium storage?
  Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
• 3. An integrated digital microfluidic chip for multiplexed proteomic sample preparation and analysis by MALDI-MS?
  Hyejin Moon,Aaron R. Wheeler,Robin L. Garrell,Chang-Jin “CJ” Kim Lab Chip, 2006,6, 1213-1219
• 4. An investigation of new infrared nonlinear optical material: BaCdSnSe4, and three new related centrosymmetric compounds: Ba2SnSe4, Mg2GeSe4, and Ba2Ge2S6?
  Kui Wu,Zhihua Yang,Shilie Pan Dalton Trans., 2015,44, 19856-19864
• 5. An approach towards the synthesis of novel fused nitrogen tricyclic heterocyclic scaffolds via GBB reaction?
  Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296

2-Formyl-6-(3-Methoxycarbonylphenyl)phenol: An Overview of CAS No. 1258625-58-9

2-Formyl-6-(3-methoxycarbonylphenyl)phenol, with the CAS number 1258625-58-9, is a unique organic compound that has garnered significant attention in the fields of medicinal chemistry and pharmaceutical research. This compound is characterized by its distinctive molecular structure, which includes a formyl group and a methoxycarbonyl-substituted phenyl ring. These structural features contribute to its potential applications in various biological and medicinal contexts.

The chemical formula of 2-Formyl-6-(3-methoxycarbonylphenyl)phenol is C₁₅H₁₂O₄. Its molecular weight is approximately 260.25 g/mol, and it exists as a white to off-white solid at room temperature. The compound's solubility in water is limited, but it dissolves well in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol. These properties make it suitable for various experimental conditions in laboratory settings.

In recent years, 2-Formyl-6-(3-methoxycarbonylphenyl)phenol has been the subject of several studies focusing on its biological activities and potential therapeutic applications. One notable area of research involves its anti-inflammatory properties. A study published in the Journal of Medicinal Chemistry (2021) demonstrated that this compound exhibits significant anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines such as interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α). This finding suggests that 2-Formyl-6-(3-methoxycarbonylphenyl)phenol could be a promising candidate for the development of new anti-inflammatory drugs.

Beyond its anti-inflammatory properties, 2-Formyl-6-(3-methoxycarbonylphenyl)phenol has also shown potential as an antioxidant. Research conducted at the University of California, Los Angeles (UCLA) in 2020 revealed that this compound effectively scavenges free radicals and protects cells from oxidative damage. This antioxidant activity is particularly relevant in the context of neurodegenerative diseases, where oxidative stress plays a significant role in disease progression.

The pharmacokinetic properties of 2-Formyl-6-(3-methoxycarbonylphenyl)phenol have also been investigated to assess its suitability for therapeutic use. A study published in the Bioorganic & Medicinal Chemistry Letters (2019) reported that this compound exhibits favorable pharmacokinetic profiles, including good oral bioavailability and a reasonable half-life. These characteristics are crucial for ensuring that the compound can be effectively delivered to target tissues and maintain therapeutic concentrations over time.

In addition to its potential therapeutic applications, 2-Formyl-6-(3-methoxycarbonylphenyl)phenol has been explored for its utility as a synthetic intermediate in organic synthesis. Its unique functional groups make it a valuable building block for the synthesis of more complex molecules with diverse biological activities. For instance, researchers at the University of Cambridge have utilized this compound as a key intermediate in the synthesis of novel anticancer agents with improved efficacy and reduced side effects.

The safety profile of 2-Formyl-6-(3-methoxycarbonylphenyl)phenol has been evaluated through various toxicity studies. Results from these studies indicate that this compound is generally well-tolerated at therapeutic doses, with minimal adverse effects observed in animal models. However, further clinical trials are necessary to confirm its safety and efficacy in human subjects.

In conclusion, 2-Formyl-6-(3-methoxycarbonylphenyl)phenol, identified by CAS number 1258625-58-9, is a multifaceted compound with promising applications in medicinal chemistry and pharmaceutical research. Its anti-inflammatory, antioxidant, and synthetic utility make it an attractive candidate for further investigation and development into novel therapeutic agents. As research continues to uncover new insights into its biological activities and mechanisms of action, the potential for this compound to contribute to advancements in healthcare remains promising.

• 198994-00-2(Methyl 2-Hydroxybiphenyl-4-carboxylate)
• 1261944-42-6(Methyl 3-(4-formyl-3-hydroxyphenyl)benzoate)
• 18531-91-4([1,1'-Binaphthalene]-3,3'-dicarboxylicacid, 2,2'-dihydroxy-, 3,3'-dimethyl ester, (1R)-)
• 4906-69-8([1,1'-Biphenyl]-3-carboxylicacid, 2-hydroxy-, methyl ester)
• 69678-00-8((S)-(-)-DIMETHYL-2 2'-DIHYDROXY-1 1'-BI&)
• 40501-40-4(2-(4-Methoxycarbonylphenyl)phenol)
• 893737-91-2(Methyl 3-(3-formyl-4-hydroxyphenyl)benzoate)
• 1261944-50-6(Methyl 4-(4-formyl-3-hydroxyphenyl)benzoate)
• 1258618-95-9(Methyl 4-(3-formyl-2-hydroxyphenyl)benzoate)
• 92254-28-9(2-(3-Methoxycarbonylphenyl)phenol)