tert-butyl N-[(5-phenylpyrimidin-2-yl)methyl]carbamate CAS 1803597-71-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1803597-71-8
Molecular FormulaC16H19N3O2
Molecular Weight285.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-butyl N-[(5-phenylpyrimidin-2-yl)methyl]carbamate CAS 1803597-71-8 chemical structure

Description

tert-butyl N-[(5-phenylpyrimidin-2-yl)methyl]carbamate (CAS 1803597-71-8), molecular formula C16H19N3O2 and molecular weight 285.34 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of tert-butyl N-[(5-phenylpyrimidin-2-yl)methyl]carbamate (C16H19N3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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. 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 tert-butyl N-[(5-phenylpyrimidin-2-yl)methyl]carbamate 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 FormulaC16H19N3O2
Molecular Weight285.34 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Nitrogen Atoms3

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