3-((4-(4,5-Dichloro-1H-imidazol-1-yl)phenyl)amino)-2-(2H-tetrazol-5-yl)acrylonitrile CAS 1024831-26-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1024831-26-2
Molecular FormulaC13H8Cl2N8
Molecular Weight347.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((4-(4,5-Dichloro-1H-imidazol-1-yl)phenyl)amino)-2-(2H-tetrazol-5-yl)acrylonitrile CAS 1024831-26-2 chemical structure

Description

The molecular framework of 3-((4-(4,5-Dichloro-1H-imidazol-1-yl)phenyl)amino)-2-(2H-tetrazol-5-yl)acrylonitrile (C13H8Cl2N8) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 3-((4-(4,5-Dichloro-1H-imidazol-1-yl)phenyl)amino)-2-(2H-tetrazol-5-yl)acrylonitrile (CAS 1024831-26-2), a certified reference material (molecular formula C13H8Cl2N8, MW 347.16 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 3-((4-(4,5-Dichloro-1H-imidazol-1-yl)phenyl)amino)-2-(2H-tetrazol-5-yl)acrylonitrile 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 FormulaC13H8Cl2N8
Molecular Weight347.16 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms8

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