| 词条 | Mesitol |
| 释义 |
| ImageFile = Mesitol_V1.svg | ImageSize = 150px | IUPACName = 2,4,6-Trimethylphenol | OtherNames = Hydroxymesitylene; Mesityl alcohol | Section1 = {{Chembox Identifiers | CASNo = 527-60-6 | PubChem = 10698 | UNII = FPZ32614N6 | ChemSpiderID = 10248 | EC_number = 208-419-2 | SMILES = Cc1cc(c(c(c1)C)O)C | StdInChI = 1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3 | StdInChIKey = BPRYUXCVCCNUFE-UHFFFAOYSA-N | Section2 = {{Chembox Properties | C=9 | H=12 | O=1 | Appearance = | Density = | MeltingPtC = 70-72 | MeltingPt_ref = [1] | BoilingPtC = 220 | BoilingPt_ref = [1] | Solubility = 1.01 g/l | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = | GHSPictograms = {{GHS05}}{{GHS09}} | GHSSignalWord = Danger | HPhrases = {{H-phrases|314|318|411}} | PPhrases = {{P-phrases|260|264|273|280|301+330+331|303+361+353|304+340|305+351+338|310|321|363|391|405|501}} }} Mesitol (2,4,6-trimethylphenol) is an aromatic chemical compound having three methyl groups and one hydroxy group. The name and structure of mesitol derives from the combination of mesitylene and phenol. Mesitol can be obtained by reaction of mesitylene with peroxomonophosphoric acid:[2] {{clear-left}} References1. ^1 {{cite web | url = https://www.sigmaaldrich.com/catalog/product/aldrich/w432900 | publisher = Sigma-Aldrich | title = 2,4,6-Trimethylphenol }} {{aromatic-stub}}2. ^{{Cite journal | doi = 10.1016/S0040-4020(01)92087-3| title = Aromatic hydroxylation with peroxymonophosphoric acid| journal = Tetrahedron| volume = 37| issue = 8| pages = 1485| year = 1981| last1 = Ogata| first1 = Yoshiro| last2 = Sawaki| first2 = Yasuhiko| last3 = Tomizawa| first3 = Kohtaro| last4 = Ohno| first4 = Takashi}} 1 : Alkylphenols |
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