TERT-BUTYL (2-IODO-6-METHYLPHENYL)CARBAMATE CAS 1447607-72-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1447607-72-8
Molecular FormulaC12H16INO2
Molecular Weight333.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

TERT-BUTYL (2-IODO-6-METHYLPHENYL)CARBAMATE CAS 1447607-72-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 333.17 g/mol gives TERT-BUTYL (2-IODO-6-METHYLPHENYL)CARBAMATE distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

TERT-BUTYL (2-IODO-6-METHYLPHENYL)CARBAMATE (CAS 1447607-72-8), molecular formula C12H16INO2 and molecular weight 333.17 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, TERT-BUTYL (2-IODO-6-METHYLPHENYL)CARBAMATE (C12H16INO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 333.17 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures TERT-BUTYL (2-IODO-6-METHYLPHENYL)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 FormulaC12H16INO2
Molecular Weight333.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentI-containing
Nitrogen Atoms1

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