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Merck
CN

B27803

Sigma-Aldrich

5-苄氧基吲哚

95%

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别名:
NSC 62895
经验公式(希尔记法):
C15H13NO
CAS号:
分子量:
223.27
Beilstein:
173532
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

95%

形式

powder

杂质

5% various solvents of crystallization

mp

100-104 °C (lit.)

SMILES字符串

C(Oc1ccc2[nH]ccc2c1)c3ccccc3

InChI

1S/C15H13NO/c1-2-4-12(5-3-1)11-17-14-6-7-15-13(10-14)8-9-16-15/h1-10,16H,11H2

InChI key

JCQLPDZCNSVBMS-UHFFFAOYSA-N

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应用

  • Reactant in regio- and stereoselective morpholine-catalyzed direct C-3 alkenylation with α,β-unsaturated aldehydes
  • Reactant in selective debenzylation of protective groups using SiliaCat-palladium under mild reaction conditions
  • Reactant in metal-free Friedel-Crafts alkylation reactions
  • Reactant in preparation of protein kinase (PKC) inhibitors
  • Reactant in preparation of indole/quinoline carbothioic acid amide derivatives

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Jeff DeFalco et al.
Bioorganic & medicinal chemistry letters, 20(23), 7076-7079 (2010-10-23)
5-Benzyloxytryptamine 19 was found to act as an antagonist of the TRPM8 ion-channel. For example, 19 had an IC(50) of 0.34 μM when menthol was used as the stimulating agonist. Related commercially-available tryptamine derivatives showed diminished, or no antagonist activity

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