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18-冠-6醚

产品号 A11249 公司名称 Alfa Aesar
CAS号 17455-13-9 公司网站 http://www.alfa.com
分子式 C12H24O6 电 话
分子量 264.31536 传 真
纯 度 99% 电子邮件
保 存 Chembase数据库ID: 75098

产品价格信息

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产品别名

标题
18-Crown-6
IUPAC标准名
1,4,7,10,13,16-hexaoxacyclooctadecane
IUPAC传统名
18-crown-6 ether
别名
1,4,7,10,13,16-Hexaoxacyclooctadecane

产品登记号

Beilstein号 1619616
EC号 241-473-5
CAS号 17455-13-9
MDL号 MFCD00005113
默克索引号 142602

产品性质

纯度 99%
沸点 116°C/0.2mm
密度 1.175
闪点 109°C(228°F)
熔点 37-41°C
GHS危险品标识 GHS07
GHS危险声明 H302-H319-H313
欧盟危险性物质标志 X
GHS警示性声明 P280-P305+P351+P338-P301+P312-P312-P337+P313-P501A
危险公开号 22-36
RTECS编号 MP4500000
安全公开号 26-36
保存注意事项 Hygroscopic
TSCA收录

产品详细信息

参考文献

  • Crown ether (see Appendix 2) mainly used to complex potassium ions. For a comprehensive study of solvent effects on complexation with K ions in a wide range of solvents, see: J. Org. Chem., 61, 5221 (1996).
  • Promotes methylation reactions with Dimethyl carbonate, A13104: Synthesis, 382 (1986). N-Alkylation of Glutarimide, L00968, and Succinimide, A13503: Bull. Soc. Chim. Fr., 227 (1992).
  • Enables KH to metallate aryl-substituted methanes directly: J. Am. Chem. Soc., 99, 4457 (1977). In the presence of KOH in DME, various arylmethanes, benzyl alcohols and aldehydes are oxidized to carboxylic acids by molecular oxygen: Tetrahedron Lett., 25, 4989 (1984).
  • Has been used with KF to enhance the reactivity of F- as a base or a nucleophile, e.g. to promote Michael additions in aprotic solvents: J. Chem. Soc., Chem. Commun., 237 (1977), the condensation of nitromethane with aldehydes: Tetrahedron Lett., 3219 (1978), and the transesterification of diaryl to dialkyl phosphonates: Synthesis, 409, 412 (1982).
  • Crown ether catalysis can be used in the reaction of KCN with alkyl halides to give nitriles: Tetrahedron Lett., 71 (1975), and for the preparation of acyl cyanides from acid chlorides: Tetrahedron Lett., 21, 2959 (1980). The 1:1 complex between 18-crown-6 and KCN has been used catalytically in the cyanosilylation of aldehydes, ketones and quinones with TMSCN; for examples, see: Org. Synth. Coll., 7, 517 (1990).
  • Has been widely used in alkylation reactions with, e.g. K2CO3 as base: