Tert-Butyl 6-Chloro-2,3-Dihydrospiro[Indene-1,4'-Piperidine]-1'-Carboxylate CAS 1160247-32-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1160247-32-4
Molecular FormulaC18H24ClNO2
Molecular Weight321.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-Butyl 6-Chloro-2,3-Dihydrospiro[Indene-1,4'-Piperidine]-1'-Carboxylate CAS 1160247-32-4 chemical structure

Description

CATO supplies Tert-Butyl 6-Chloro-2,3-Dihydrospiro[Indene-1,4'-Piperidine]-1'-Carboxylate (CAS 1160247-32-4), a certified reference material (molecular formula C18H24ClNO2, MW 321.84 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, Tert-Butyl 6-Chloro-2,3-Dihydrospiro[Indene-1,4'-Piperidine]-1'-Carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 321.84 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.

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.

Physical & Chemical Properties

Molecular FormulaC18H24ClNO2
Molecular Weight321.84 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms1

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