2-(4-(Iodomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane CAS 1169945-44-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1169945-44-1
Molecular FormulaC13H18BIO2
Molecular Weight344.00 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-(Iodomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane CAS 1169945-44-1 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

2-(4-(Iodomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS 1169945-44-1), molecular formula C13H18BIO2 and molecular weight 344.00 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system, 2-(4-(Iodomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 344.00 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

Physical & Chemical Properties

Molecular FormulaC13H18BIO2
Molecular Weight344.00 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentI-containing

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Why CATO?