[B21810] CAS 15861-24-2 | Indole-5-carbonitrile, 98+% | Alfa
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Brand: Alfa Aesar
15861-24-2 | C9H6N2 | indole-5-cyano-
Chemical Identifiers
CAS
15861-24-2
Molecular Weight (g/mol)
142.16
Synonym
indole-5-cyano-
SMILES
N#CC1=CC=C2NC=CC2=C1
InChI Key
YHYLDEVWYOFIJK-UHFFFAOYSA-N
Molecular Formula
C9H6N2
IUPAC Name
1H-indole-5-carbonitrile
Specifications
Form
Powder
Assay (GC)
≥98.0%
Melting Point (clear melt)
103.0-109.0?C
Appearance (Color)
White to cream to yellow
설명
Reactant used for parallel synthesis of dihydroisoquinolines via silver and L-proline co-catalyzed three-component coupling reaction, preparation of novel PPARα/γ dual agonists for potential treatment of metabolic syndrome and IDDM, chemo selective and regioselective preparation of benzoyl indoles, 4,5-dihydrocyclopenta[c]quinolines by palladium-catalyzed ring-expansion reaction alkynes, using O2 as the oxidant and vinylindoles by hydroarylation of alkynes using indium bromide catalyst.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Reactant used for parallel synthesis of dihydroisoquinolines via silver and L-proline co-catalyzed three-component coupling reaction, preparation of novel PPARα/γ dual agonists for potential treatment of metabolic syndrome and IDDM, chemo selective and regioselective preparation of benzoyl indoles, 4,5-dihydrocyclopenta[c]quinolines by palladium-catalyzed ring-expansion reaction alkynes, using O2 as the oxidant and vinylindoles by hydroarylation of alkynes using indium bromide catalyst.
Reactant used for parallel synthesis of dihydroisoquinolines via silver and L-proline co-catalyzed three-component coupling reaction, preparation of novel PPARα/γ dual agonists for potential treatment of metabolic syndrome and IDDM, chemo selective and regioselective preparation of benzoyl indoles, 4,5-dihydrocyclopenta[c]quinolines by palladium-catalyzed ring-expansion reaction alkynes, using O2 as the oxidant and vinylindoles by hydroarylation of alkynes using indium bromide catalyst.
Solubility
Soluble in chloroform, hexane and methanol. Insoluble in water.
Notes
Light Sensitive, store in dark. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
Other References:
Beilstein:116738
GHS Hazard and Precautionary Statements
Hazard Statements:H302+H312+H332-H315-H319-H335
GHS H StatementH302-H315-H319-H335Harmful if swallowed.Causes skin irritation.Causes serious eye irritation.May cause respiratory irritation.
Precautionary Statements:P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
Risk & Safety
TSCA:NoRTECS Number:NL5993120
경고:RUO – Research Use Only
CAS15861-24-2FORMULAC9H6N2HAZARD CLASS6.1EINECS239-986-4MDLMFCD00005669PACKAGING GROUPIII
| Pakage | 1g, 5g |
|---|---|
| brand | Alfa Aesar |
