6-Nitro-1-(4-(trifluoromethyl)phenyl)-1H-indazole CAS 838820-86-3

Purity 97%+In StockPharmaceutical Standards
CAS No.838820-86-3
Molecular FormulaC14H8F3N3O2
Molecular Weight307.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Nitro-1-(4-(trifluoromethyl)phenyl)-1H-indazole CAS 838820-86-3 chemical structure

Description

6-Nitro-1-(4-(trifluoromethyl)phenyl)-1H-indazole (CAS 838820-86-3), molecular formula C14H8F3N3O2 and molecular weight 307.23 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C14H8F3N3O2, 6-Nitro-1-(4-(trifluoromethyl)phenyl)-1H-indazole contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 307.23 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures 6-Nitro-1-(4-(trifluoromethyl)phenyl)-1H-indazole 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 FormulaC14H8F3N3O2
Molecular Weight307.23 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentF-containing
Nitrogen Atoms3

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Why CATO?