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Thermo Scientific Chemicals
4-Methylbenzyl alcohol, 99%
CAS: 589-18-4 | C8H10O | 122.167 g/mol
化学物質識別子
CAS589-18-4
IUPAC Name(4-methylphenyl)methanol
Molecular FormulaC8H10O
InChI KeyKMTDMTZBNYGUNX-UHFFFAOYSA-N
SMILESCC1=CC=C(CO)C=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)White
FormCrystals or powder or crystalline powder
Assay (GC)≥98.5%
Melting Point (clear melt)56.5-62.5?C
4-Methylbenzyl alcohol is used in fragrances, flavoring and as a laboratory reagent. It is also used as a raw material for the preparation of polycarbonates and 4-methyl-benzaldehyde.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-Methylbenzyl alcohol is used in fragrances, flavoring and as a laboratory reagent. It is also used as a raw material for the preparation of polycarbonates and 4-methyl-benzaldehyde.
Solubility
Soluble in methanol, ether and ethanol. Slightly soluble in water.
Notes
Incompatible with oxidizing agents, acids, acid chlorides and acid anhydrides.
4-Methylbenzyl alcohol is used in fragrances, flavoring and as a laboratory reagent. It is also used as a raw material for the preparation of polycarbonates and 4-methyl-benzaldehyde.
Solubility
Soluble in methanol, ether and ethanol. Slightly soluble in water.
Notes
Incompatible with oxidizing agents, acids, acid chlorides and acid anhydrides.
RUO – Research Use Only
General References:
- A high yield modification of the Ritter conversion of benzyl alcohols to N-acetylbenzylamines is illustrated by the reaction of this alcohol with acetonitrile in the presence of BF 3 etherate to give N-acetyl-4-methylbenzylamine: Synth. Commun., 24, 601 (1994).
- Choo, G. C. Y.; Miyamura, H.; Kobayashi, S. Synergistic cascade catalysis by metal nanoparticles and Lewis acids in hydrogen autotransfer. Chem. Sci. 2015, 6, 1719-1727.
- Maurya, C. K.; Gupta, P. K. Decarbamoylation of primary carbamates using sodium in silica gel (Na_SG). Tetrahedron Lett. 2015, 56 (17), 2228-2230.