Phenol

News Phenol

• 'Tricking' bacteria into hydroxylating benzene
  

  Breaking carbon-hydrogen bonds is notoriously difficult in lab chemistry, yet nature does it effortlessly. Now, scientists have used E.coli bacteria to oxidize the C-H bonds in benzene to generate phenol, with a genetically inserted enzyme (cytochrome P450BM3), that originally evolved to target othe more

• SONGWON begins large scale manufacture of functional monomers

  Having started to develop functional monomers about two years ago, SONGWON has now begun bulk manufacture at its production site in Ulsan, South Korea. These monomers provide resins and polymers with special functions, one of the most important being improvement of the physical and chemical properti more

• A way to synthesize drugs from renewable precursors
  

  The scientists of RUDN University together with their Russian colleagues have developed a new approach to the synthesis of benzofurans from cheap raw materials. Original furans can be produced from wastes of agriculture and wooworking industry, such as sawdust, cobs and other by-products of crop pro more

Infographics Phenol

The Chemistry Behind the Smell of Wet Dogs

If you’re a dog owner, hot weather inevitably leads to wet dogs, particularly if you live near the sea, a river, or basically any other body of water that looks appealing to your canine companion. It’s probably not escaped your notice that dogs tend to smell pretty awful after getting wet. Why is th more

Benzene Derivatives in Organic Chemistry

Benzene is a hugely important compound in organic chemistry. It consists of six carbon atoms joined together in a ring, with a hydrogen atom bonded to each carbon; by replacing one or more of these hydrogens with a functional group, a large number of different compounds can be formed. This graphic l more

Publications Phenol

• “Tubular J-Aggregates of a New Thiacarbocyanine Cy5 Dye for the Far-red Spectral Region – A Spectroscopic and Cryo-Transmission Electron Microscopy Study”

  The aggregation behavior of a phenol-substituted thiacarbocyanine Cy5 dye (5-chloro-2-[5-[5-chloro-3-(4-sulfobutyl)-3H-benzothiazol-2-ylidene]-3-phenyl-penta-1,3-dienyl]-3-(4-sulfo¬butyl)-benzothiazol-3-ium hydroxide, inner salt, triethylammonium salt) in aqueous solution is investigated using stead more

• Tetranuclear and dinuclear phenoxido bridged copper complexes based on unsymmetrical thiosemicarbazone ligands

  We report on the synthesis of new dinucleating phenol-based “end-off” compartmental ligands HLMeH and HLMe2 bearing two different binding sites, one bis(2-methylpyridyl)aminomethyl (BPA) and one thiosemicarbazone (TSC) site, and their corresponding copper(II) complexes 1t and 2d. With the ligand HLM more

• Molecules, Vol. 23, Pages 1577: New Bisabosquals from Stachybotrys sp. PH30583 Elicited on Solid Media

  Molecules, Vol. 23, Pages 1577: New Bisabosquals from Stachybotrys sp. PH30583 Elicited on Solid Media Molecules doi: 10.3390/molecules23071577 Authors: Bao-Hui Ruan Shu-Quan Li Xue-Qiong Yang Ya-Bin Yang Ya-Mei Wu Li-Jiao Shi Hai-Yue Yin Hao Zhou Zhong-Tao Ding Stachy more