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567701 Aldrich

(5-Benzyloxyindol-3-yl)acetonitrile

97%

Synonym: 5-Benzyloxyindole-3-acetonitrile, NSC 73391

  • CAS Number 2436-15-9

  • Empirical Formula (Hill Notation) C17H14N2O

  • Molecular Weight 262.31

  •  MDL number MFCD00022730

  •  PubChem Substance ID 24880386

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Properties

Related Categories Building Blocks, C13 to C27, Chemical Synthesis, Heterocyclic Building Blocks, Indoles More...
InChI Key   ADPRFNVFBYHCJQ-UHFFFAOYSA-N
assay   97%
mp   76-80 °C(lit.)

Description

Packaging

5 g in glass bottle

Application

• Reactant for preparation of of β-carboline derivatives as antioxidants in the LDL oxidation model
• Reactant for preparation of indole-N-acetic acid derivatives as aldose reductase inhibitors for diabetic complications treatment
• Reactant for preparation of tryptamine analogs as antihypertensive agents

Price and Availability

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Protocols & Articles

Articles

Indoles

Sigma-Aldrich is proud to offer a new series of ChemFiles—called Privileged Structures, to our Drug Discovery and Organic Synthesis customers. Each piece will highlight a specific motif, selected app...
Chemfiles Volume 4 Article 8
Keywords: Applications, Building blocks, Cardiovascular, Chemfiles, Company, Diabetes, Diseases, Drug discovery, Medicinal chemistry, Organic synthesis, Respiratory

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Indoles, Purines, and Their Isosteres

Substituted indoles and purines have frequently been referred to as “privileged structures” since they are capable of binding to multiple receptors with high affinity, and thus have applications acro...
Keywords: Building blocks, Medicinal chemistry

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