2-(Aminomethyl)-3-(difluoromethyl)-5-iodo-4-(trifluoromethyl)pyridine CAS 1806987-43-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1806987-43-8
Molecular FormulaC8H6F5IN2
Molecular Weight352.04 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Aminomethyl)-3-(difluoromethyl)-5-iodo-4-(trifluoromethyl)pyridine CAS 1806987-43-8 chemical structure

Description

Structurally, 2-(Aminomethyl)-3-(difluoromethyl)-5-iodo-4-(trifluoromethyl)pyridine (C8H6F5IN2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 352.04 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.

2-(Aminomethyl)-3-(difluoromethyl)-5-iodo-4-(trifluoromethyl)pyridine (CAS 1806987-43-8), molecular formula C8H6F5IN2 and molecular weight 352.04 g/mol, is a CATO reference standard with documented purity and traceability.

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 2-(Aminomethyl)-3-(difluoromethyl)-5-iodo-4-(trifluoromethyl)pyridine 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 FormulaC8H6F5IN2
Molecular Weight352.04 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentF/I-containing
Nitrogen Atoms2

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