n-[2-(1h-1,3-benzodiazol-2-yl)ethyl]-4-fluoro-2-nitroaniline CAS 1356752-29-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1356752-29-8
Molecular FormulaC15H13FN4O2
Molecular Weight300.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-[2-(1h-1,3-benzodiazol-2-yl)ethyl]-4-fluoro-2-nitroaniline CAS 1356752-29-8 chemical structure

Description

n-[2-(1h-1,3-benzodiazol-2-yl)ethyl]-4-fluoro-2-nitroaniline (CAS 1356752-29-8) is a high-purity analytical reference standard with the molecular formula C15H13FN4O2 and a molecular weight of 300.29 g/mol.

Structurally, n-[2-(1h-1,3-benzodiazol-2-yl)ethyl]-4-fluoro-2-nitroaniline (C15H13FN4O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 300.29 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 n-[2-(1h-1,3-benzodiazol-2-yl)ethyl]-4-fluoro-2-nitroaniline 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 FormulaC15H13FN4O2
Molecular Weight300.29 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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.)1991
Halogen ContentF-containing
Nitrogen Atoms4

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