2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazine CAS 866089-28-3

Purity 97%+In StockPharmaceutical Standards
CAS No.866089-28-3
Molecular FormulaC10H13NO
Molecular Weight163.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazine CAS 866089-28-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazine.

CATO supplies 2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazine (CAS 866089-28-3), a certified reference material (molecular formula C10H13NO, MW 163.22 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazine is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 163.22 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazine 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 FormulaC10H13NO
Molecular Weight163.22 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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