Newblue-CHEM 1215-...

Newblue-CHEM 1215-59-4 5-Benzyloxyindole

Newblue-CHEM 1215-59-4 5-Benzyloxyindole

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1 Kilogram

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  • Min.Order :1 Kilogram
  • Purity: 99%min
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Keywords

1215-59-4 5-Benzyloxyindole C15H13NO

Quick Details

  • Appearance:conform
  • Application:1215-59-4
  • PackAge:normal package
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:conform
  • Transportation:by air

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Details:

5-Benzyloxyindole Basic information
Product Name: 5-Benzyloxyindole
Synonyms: 5-(Phenylmethoxy)-1H-indole;5-benzyloxy-indol;Benzyloxy-5 indole;Indole, 5-(benzyloxy)-;TIMTEC-BB SBB003331;BENZYLOXYINDOLE(5-);5-BENZYLOXY-1H-INDOLE;5-BENZYLOXYINDOLE
CAS: 1215-59-4
MF: C15H13NO
MW: 223.27
EINECS: 214-930-1
Product Categories: blocks;IndolesOxindoles;Indoles and derivatives;Pyrroles & Indoles;Indoline & Oxindole;Indole Series;Indoles;Simple Indoles;Indole;Pyrroles & Indoles;Building Blocks;Heterocyclic Building Blocks;Aromatics;Indole Derivatives;Heterocycle-Indole series
Mol File: 1215-59-4.mol
5-Benzyloxyindole Structure
 
5-Benzyloxyindole Chemical Properties
mp  100-104 °C(lit.)
storage temp.  2-8°C
solubility  ethanol: may be hazy yellow
form  powder
color  white to light yellow
BRN  173532
CAS DataBase Reference 1215-59-4(CAS DataBase Reference)
NIST Chemistry Reference 1H-indole, 5-(phenylmethoxy)-(1215-59-4)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-24/25-22
WGK Germany  3
RTECS  NL4850000
F  8-10
Hazard Note  Irritant
HazardClass  IRRITANT
HS Code  29339990
MSDS Information
Provider Language
5-(Benzyloxy)-1H-indole English
SigmaAldrich English
ACROS English
ALFA English
 
5-Benzyloxyindole Usage And Synthesis
Chemical Properties Off-white to beige powder
Usage 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.

 

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