6-Chloro-2-ethyl-1-methyl-1H-indole-3-carboxylic acid CAS 1784299-01-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1784299-01-9
Molecular FormulaC12H12ClNO2
Molecular Weight237.68 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Chloro-2-ethyl-1-methyl-1H-indole-3-carboxylic acid CAS 1784299-01-9 chemical structure

Description

Structurally, 6-Chloro-2-ethyl-1-methyl-1H-indole-3-carboxylic acid (C12H12ClNO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 237.68 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies 6-Chloro-2-ethyl-1-methyl-1H-indole-3-carboxylic acid (CAS 1784299-01-9), a certified reference material (molecular formula C12H12ClNO2, MW 237.68 g/mol) for analytical method development and quality control.

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 6-Chloro-2-ethyl-1-methyl-1H-indole-3-carboxylic acid 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 FormulaC12H12ClNO2
Molecular Weight237.68 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentCl-containing
Nitrogen Atoms1

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