1-(1,2-Propadienyl)-1h-indole-3-carbaldehyde CAS 923203-33-2

Purity 97%+In StockPharmaceutical Standards
CAS No.923203-33-2
Molecular FormulaC12H9NO
Molecular Weight183.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(1,2-Propadienyl)-1h-indole-3-carbaldehyde CAS 923203-33-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 183.21 g/mol gives 1-(1,2-Propadienyl)-1h-indole-3-carbaldehyde distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 1-(1,2-Propadienyl)-1h-indole-3-carbaldehyde (CAS 923203-33-2), a certified reference material (molecular formula C12H9NO, MW 183.21 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H9NO, 1-(1,2-Propadienyl)-1h-indole-3-carbaldehyde contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 183.21 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 1-(1,2-Propadienyl)-1h-indole-3-carbaldehyde under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H9NO
Molecular Weight183.21 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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