物质信息

ID:717105

名称和标识
IUPAC标准名
pyridin-2-ol
IUPAC传统名
2-pyridone
别名
2-Hydroxypyridine2-羟基吡啶2(1H)-Pyridone2-Pyridinol
数据登录号
CAS号
Beilstein号
化合物性质
安全信息
联合国危险货物编号
UN2811
联合国危险货物包装类别(PG)
III
GHS危险声明
H301-H315-H319-H335
TSCA收录
RTECS编号
UV1144050
联合国危险货物等级
6.1
GHS警示性声明
P261-P301+P310-P305+P351+P338-P302+P352-P405-P501A
GHS危险品标识
GHS06
急性毒性(口服,皮肤接触,吸入),类别1,2,3
欧盟危险性物质标志
有毒 有毒 (T)
安全公开号
26-36/37-45
危险公开号
25-36/37/38
产品相关信息
纯度
98+%
理化性质
熔点
102-111°C
密度
1.39
闪点
210°C(410°F)
沸点
280-281°C
描述信息
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分子图谱
暂无数据
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参考文献
• Bifunctional catalyst for a wide variety of acylation reactions. See, for example: J. Chem. Soc. (C), 89 (1969).
• Reacts with SOCl2 to form di-2-pyridyl sulfite, a useful reagent for in situ formation of N-sulfinylamines, nitriles, isocyanides and carbodiimides under mild conditions: Tetrahedron Lett., 27, 1925 (1986).
• For use of 2-pyridyl esters as active esters in peptide coupling, see: J. Chem. Soc.(C), 2896 (1971); Chem. Ber., 118, 468 (1985). The group can be introduced on to the N-protected peptide using DCC in pyridine, and is displaced by the amino-residue under mild conditions. For peptide reagents, see Appendix 6. Similar methodology has also been used in an improved preparation of trichloroethyl esters: Synthesis, 24 (1979).