• 1. Excited-state proton-coupled electron transfer within ion pairs?
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• 2. Fe/Fe3C@C nanoparticles encapsulated in N-doped graphene–CNTs framework as an efficient bifunctional oxygen electrocatalyst for robust rechargeable Zn–air batteries?
  Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
• 3. Excitonic and vibrational coherence in artificial photosynthetic systems studied by negative-time ultrafast laser spectroscopy
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• 4. Dissociation of large gaseous serine clusters produces abundant protonated serine octamer
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• 5. Excited state dynamics of symmetric and asymmetric Cr3(dpa)4Cl2 measured using femtosecond transient absorption spectroscopy?
  Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Phenylpropanes

Benzenepropanol, 4-(1,1-Dimethylethyl)-b-Methyl

Benzenepropanol, 4-(1,1-Dimethylethyl)-b-Methyl, also known by its CAS registry number CAS No. 56107-04-1, is a versatile organic compound with significant applications in various industries. This compound is a derivative of benzene, a fundamental aromatic hydrocarbon, and exhibits unique chemical properties due to its substituents. The presence of the propanol group and the bulky tert-butyl group at the para position of the benzene ring imparts distinctive reactivity and physical characteristics to this molecule.

The molecular formula of Benzenepropanol, 4-(1,1-Dimethylethyl)-b-Methyl is C₁₃H₂₂O, and its molecular weight is approximately 198.3 g/mol. The compound exists as a colorless liquid with a characteristic odor. Its physical properties, such as melting point and boiling point, are influenced by the steric hindrance introduced by the tert-butyl group. The melting point is around -5°C, while the boiling point is reported to be 95°C at standard atmospheric pressure.

Benzenepropanol, 4-(1,1-Dimethylethyl)-b-Methyl is widely used in the chemical industry as an intermediate in the synthesis of more complex organic compounds. Its structure makes it an ideal candidate for various reactions, including oxidation, reduction, and condensation processes. Recent studies have highlighted its potential as a precursor in the production of pharmaceutical intermediates and agrochemicals.

In terms of chemical synthesis, Benzenepropanol, 4-(1,1-Dimethylethyl)-b-Methyl can be prepared through several routes. One common method involves the alkylation of phenol derivatives using alkyl halides in the presence of a strong base. Another approach utilizes Grignard reagents to introduce the tert-butyl group onto the aromatic ring. These methods have been optimized in recent years to improve yield and selectivity.

The compound's applications extend beyond its role as an intermediate. It has been employed in the formulation of fragrances due to its pleasant odor profile. Additionally, it serves as a solvent in certain industrial processes where its high boiling point and moderate polarity are advantageous.

Benzenepropanol, 4-(1,1-Dimethylethyl)-b-Methyl has also garnered attention in academic research for its potential in green chemistry applications. Researchers have explored its use in catalytic processes that promote sustainability by reducing waste and improving energy efficiency.

In conclusion, CAS No. 56107-04-1, or Benzenepropanol, 4-(1,1-Dimethylethyl)-b-Methyl, is a multifaceted compound with diverse applications across various sectors. Its unique chemical structure and properties make it an invaluable tool in modern organic synthesis and industrial processes.

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