2-((Tert-butoxycarbonyl)amino)-4-methoxybenzoic acid CAS 136247-96-6

Purity 97%+In StockPharmaceutical Standards
CAS No.136247-96-6
Molecular FormulaC13H17NO5
Molecular Weight267.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((Tert-butoxycarbonyl)amino)-4-methoxybenzoic acid CAS 136247-96-6 chemical structure

Description

Structurally, 2-((Tert-butoxycarbonyl)amino)-4-methoxybenzoic acid (C13H17NO5) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 267.28 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

2-((Tert-butoxycarbonyl)amino)-4-methoxybenzoic acid (CAS 136247-96-6) is a high-purity analytical reference standard with the molecular formula C13H17NO5 and a molecular weight of 267.28 g/mol.

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-((Tert-butoxycarbonyl)amino)-4-methoxybenzoic acid 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 FormulaC13H17NO5
Molecular Weight267.28 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Nitrogen Atoms1

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