4-Fluoroisoindolin-5-ol CAS 1447694-54-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1447694-54-3
Molecular FormulaC8H8FNO
Molecular Weight153.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Fluoroisoindolin-5-ol CAS 1447694-54-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 153.15 g/mol gives 4-Fluoroisoindolin-5-ol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-Fluoroisoindolin-5-ol (CAS 1447694-54-3) is a high-purity analytical reference standard with the molecular formula C8H8FNO and a molecular weight of 153.15 g/mol.

4-Fluoroisoindolin-5-ol (C8H8FNO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 4-Fluoroisoindolin-5-ol 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 FormulaC8H8FNO
Molecular Weight153.15 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Nitrogen Atoms1

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