3,3,5-三甲基己醇
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IUPAC名 3,5,5-Trimethyl-1-hexanol
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识别
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CAS号
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3452-97-9
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ChemSpider
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17881
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SMILES
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InChI
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- 1S/C9H20O/c1-8(5-6-10)7-9(2,3)4/h8,10H,5-7H2,1-4H3
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EINECS
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222-376-7
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ChEBI
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178388
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MeSH
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3,5,5-trimethyl-1-hexanol
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性质
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化学式
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C9H20O
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摩尔质量
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144.25 g·mol−1
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外观
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澄清液体
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氣味
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herbaceous, plant-like [1]
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密度
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0.824 g/mL
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熔点
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-70 °C
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沸点
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194.0 °C
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溶解性(水)
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0.45 g/L
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溶解性
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Soluble in alcohol, acetone, ester
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蒸氣壓
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0.2 torr
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kH
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4.12·10-5 atm m3 / mol
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危险性
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GHS危险性符号
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GHS提示词
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警告
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H-术语
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H227, H315, H319, H373, H411
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P-术语
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P210, P260, P264, P273, P280, P302+352, P305+351+338, P314, P332+313, P337+313, P362, P370+378, P391, P403+235
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闪点
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80°C
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相关物质
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相关化学品
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7-甲基辛醇
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若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。
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3,3,5-三甲基己醇是一种有机化合物,化学式为C9H20O,它可以三(2,4,4-三甲基戊基)硼为原料得到。[2]它和对甲苯磺酰氯反应,可以得到对甲苯磺酸-3,5,5-三甲基己酯。[3]在三苯基膦存在下,它和N-溴代丁二酰亚胺反应,可以得到1-溴-3,5,5-三甲基己烷。[4]
参考文献
- ^ Lee, G. H.; Shin, Y.; Oh, M. J. Aroma-active components of Lycii fructus (kukija). Journal of Food Science. 2008, 73 (6): C500–505 [2022-03-05]. ISSN 0022-1147. PMID 19241541. doi:10.1111/j.1750-3841.2008.00851.x. (原始内容存档于2022-03-02).
- ^ Ei-Ichi Negishi, Michael J. Idacavage. John Wiley & Sons, Inc. , 编. Formation of CarbonCarbon and CarbonHeteroatom Bonds via Organoboranes and Organoborates. Hoboken, NJ, USA: John Wiley & Sons, Inc. 1985-01-04: 1–246 [2022-03-05]. ISBN 9780471264187. doi:10.1002/0471264180.or033.01. (原始内容存档于2022-03-08) (英语).
- ^ Bin Xu, Uttam K. Tambar. Remote Allylation of Unactivated C(sp 3 )–H Bonds Triggered by Photogenerated Amidyl Radicals. ACS Catalysis. 2019-05-03, 9 (5): 4627–4631 [2022-03-05]. ISSN 2155-5435. PMC 8186322 . PMID 34109055. doi:10.1021/acscatal.9b00563. (原始内容存档于2022-03-05) (英语).
- ^ Paul R. Frail, Kimihiro Susumu, Michael Huynh, Jennie Fong, J. M. Kikkawa, Michael J. Therien. Modulation of Dark Conductivity over a 1 × 10 −12 to 1 × 10 −5 S/cm Range Through Ancillary Group Modification in Amorphous Solids of Ethyne-Bridged (Porphinato)zinc(II) Oligomers. Chemistry of Materials. 2007-12-01, 19 (25): 6062–6064 [2022-03-05]. ISSN 0897-4756. doi:10.1021/cm701914a. (原始内容存档于2022-03-05) (英语).
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