Methyl (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-iodobutanoate CAS 1323995-10-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1323995-10-3
Molecular FormulaC20H20INO4
Molecular Weight465.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-iodobutanoate CAS 1323995-10-3 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies Methyl (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-iodobutanoate (CAS 1323995-10-3), a certified reference material (molecular formula C20H20INO4, MW 465.28 g/mol) for analytical method development and quality control.

Structurally, Methyl (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-iodobutanoate (C20H20INO4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 465.28 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures Methyl (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-iodobutanoate 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 FormulaC20H20INO4
Molecular Weight465.28 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentI-containing
Nitrogen Atoms1

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