3,4-Dihydro-2H-benzo[b][1,4]oxazin-7-ol hydrochloride CAS 1149370-96-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1149370-96-6
Molecular FormulaC8H9NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Dihydro-2H-benzo[b][1,4]oxazin-7-ol hydrochloride CAS 1149370-96-6 chemical structure

Description

Structurally, 3,4-Dihydro-2H-benzo[b][1,4]oxazin-7-ol hydrochloride (C8H9NO2HCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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 187.62 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

3,4-Dihydro-2H-benzo[b][1,4]oxazin-7-ol hydrochloride (CAS 1149370-96-6), molecular formula C8H9NO2HCl and molecular weight 187.62 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 3,4-Dihydro-2H-benzo[b][1,4]oxazin-7-ol hydrochloride 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 FormulaC8H9NO2 HCl
Molecular Weight187.62 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms1

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