物质信息

ID:714092

名称和标识
IUPAC标准名
adamantan-1-ol
IUPAC传统名
1-hydroxyadamantane
别名
1-Adamantanol1-Hydroxyadamantane1-金刚醇
数据登录号
Beilstein号
CAS号
化合物性质
产品相关信息
纯度
99%
安全信息
TSCA收录
RTECS编号
AU4980000
理化性质
熔点
ca 245°C subl.
描述信息
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分子图谱
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参考文献
• Reaction with Hydrogen fluoride pyridine complex, L17117, gives 1-fluoroadamantane, a general method for conversion of sec- and tert-alcohols to fluoroalkanes: Org. Synth. Coll., 6, 628 (1988).
• Carboxyl groups of amino acids have been protected as 1-adamantyl esters via the amino acid tosylate and dimethyl sulfite. The group is readily cleaved with TFA under mild conditions: Synthesis, 1355 (1996). Has also been applied in blocking the ?-carboxyl group of aspartic acid in peptide synthesis; the 1-adamantyl ester is prepared using DCC-DMAP: J. Chem. Soc., Perkin 1, 2129 (1988). See also Appendix 6.
• Thiol groups may also be protected by formation of the thioether in TFA. Cleavage is by means of Hg(II) salts: Chem. Pharm. Bull., 26, 1576 (1978).