
2-tert-Butyl-4-methylphenol | CAS:2409-55-4
2-tert-Butyl-4-methylphenol
- 名称:2-叔丁基对甲苯酚; 2-叔丁基-4-甲酚; 2-叔丁基-4-甲基苯酚; 2-叔丁基对甲酚; 2-(1,1-二甲基乙基)-4-甲基苯酚; 2-特丁基-4-甲基苯酚; 邻叔丁基对甲酚 | 2-tert-Butyl-4-methylphenol
- CAS号:2409-55-4
- 别名:2-tert-Butyl-p-cresol; 6-tert-Butyl-4-methylphenol; 6-tert-Butyl-p-methylphenol; 6-tert-Butyl-4-cresol; 6-tert-Butyl-p-cresol; 1-Hydroxy-2-tert-butyl-4-methylbenzene; 2-(1,1-Dimethylethyl)-4-methylphenol
- 分子式:C11H16O
- 分子量:164.25
- EINESC号:219-314-6
产品描述
物理化学性质
熔点 | 50-53 ºC |
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水溶性 | 不溶 |
沸点 | 237 ºC |
闪点 | 105 ºC |
安全数据
危险品标志 | C;N |
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危险类别码 | R34;R51/53 |
安全说明书 | S26;S29;S36/37/39;S45;S61 |
产品合成路线
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同行评议文献
Detoxication of the 2',3'-epoxide metabolites of allylbenzene and estragole. Conjugation with glutathione.G Luo et al.Drug metabolism and disposition: the biological fate of chemicals, 22(5), 731-737 (1994-09-01)
Investigation of the role of the 2',3'-epoxidation pathway in the bioactivation and genotoxicity of dietary allylbenzene analogs.T M Guenthner et al.Toxicology, 160(1-3), 47-58 (2001-03-14)
Covalent binding to DNA in vitro of 2',3'-oxides derived from allylbenzene analogs.G Luo et al.Drug metabolism and disposition: the biological fate of chemicals, 24(9), 1020-1027 (1996-09-01)
备注
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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