127809
4-甲基苯甲醇
98%
别名:
4-甲基苯甲醇, 对甲基苄醇, 对甲苯基甲醇, （4-甲基苯基）甲醇, （4-甲苯基）甲醇
方案
98%
沸点
217 °C (lit.)
mp
59-61 °C (lit.)
官能团
hydroxyl
SMILES字符串
Cc1ccc(CO)cc1
InChI
1S/C8H10O/c1-7-2-4-8(6-9)5-3-7/h2-5,9H,6H2,1H3
InChI key
KMTDMTZBNYGUNX-UHFFFAOYSA-N
一般描述
4-甲基苯甲醇广泛用于调味剂和香料。被用于合成醛和聚碳酸酯的前体。
应用
4-甲基苄醇可用于制备聚碳酸酯。它也可用于合成醇。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Selective Oxidation of Benzyl alcohols to Benzaldyhydes under Phase Transfer Catalysis
Chemical Science Review and Letters, 3, 123-126 (2014)
Carla Villa et al.
International journal of cosmetic science, 30(2), 139-144 (2008-04-02)
Several alcohols--interesting as cosmetic fragrances whose main preparative route on an industrial scale or in the research laboratory is the reduction of the corresponding carbonyl compound--were obtained by a solvent-free methodology in a green chemistry context. The process involves the
Bryce V Plapp et al.
Archives of biochemistry and biophysics, 701, 108825-108825 (2021-03-07)
Enzymes typically have high specificity for their substrates, but the structures of substrates and products differ, and multiple modes of binding are observed. In this study, high resolution X-ray crystallography of complexes with NADH and alcohols show alternative modes of
Koichiro Mikami et al.
Journal of the American Chemical Society, 135(18), 6826-6829 (2013-05-01)
An organocatalyzed ring-opening polymerization methodology was developed for the preparation of polycarbonates derived from glucose as a natural product starting material. The cyclic 4,6-carbonate monomer of glucose having the 1, 2, and 3 positions methyl-protected was prepared in three steps
Hironao Sajiki et al.
Chemical & pharmaceutical bulletin, 51(3), 320-324 (2003-03-04)
Employment of a Pd/C-pyridine combination as a catalyst is a very useful method for the selective removal (hydrogenolysis) of phenolic O-benzyl, N-Cbz and benzyl ester protective groups and for the selective hydrogenation of nitro and olefin functions of phenol derivatives
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