CAS 1687-61-2
:2-éthyl-5-méthylphénol
- 2-Ethyl-5-Methylphenol
- Brn 2042212
- Ethyl-m-cresol
- Phenol, 2-ethyl-5-methyl-
- m-Cresol, 6-ethyl-
Phenol, 2-ethyl-5-methyl-
CAS :Formule :C9H12ODegré de pureté :98%Couleur et forme :LiquidMasse moléculaire :136.19102-Ethyl-5-methylphenol
CAS :2-Ethyl-5-methylphenolDegré de pureté :≥98%Masse moléculaire :136.19g/mol2-Ethyl-5-methylphenol
CAS :2-Ethyl-5-methylphenol is an alkylphenol that can be isolated or identified from Penicillium aurantiogriseum, P. verrucosum and P. viridicatum.Formule :C9H12ODegré de pureté :99.71%Couleur et forme :SolidMasse moléculaire :136.192-Ethyl-5-methylphenol
CAS :Produit contrôléApplications 2-Ethyl-5-methylphenol (cas# 1687-61-2) is useful for the characterization of bio-oil from hardwood and softwood lignin via pyrolysis.
References Zadeh, Z. E., et al.: Energies (Basel, Switzerland), 13, 887 (2020)Formule :C9H12OCouleur et forme :NeatMasse moléculaire :136.192-Ethyl-5-methylphenol
CAS :2-Ethyl-5-methylphenol is a natural product that belongs to the class of phenols. It is biosynthesized by the conversion of 2-methylacetophenone, which is found in styrene and exocrine glands in arachnids. This compound has been shown to be toxic to a number of bacteria, including strains resistant to antibiotics such as methicillin and cephalothin. The toxicity of 2-ethyl-5-methylphenol against bacteria may be due to its ability to inhibit protein synthesis and disrupt cellular membranes. The pathways leading from 2-methylacetophenone to 2-ethyl-5-methylphenol involve two steps: nitration followed by ethylation.
2E5MP can be synthesized using acetone and 3- methyl1 -butanol as precursors, which are scalable and inexpensive chemicals.Formule :C9H12ODegré de pureté :Min. 95%Masse moléculaire :136.19 g/mol




