Endo-(1s)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl chloroacetate CAS 75556-46-6

Purity 97%+In StockPharmaceutical Standards
CAS No.75556-46-6
Molecular FormulaC12H19ClO2
Molecular Weight230.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Endo-(1s)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl chloroacetate CAS 75556-46-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 230.73 g/mol gives Endo-(1s)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl chloroacetate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Endo-(1s)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl chloroacetate (CAS 75556-46-6) is a high-purity analytical reference standard with the molecular formula C12H19ClO2 and a molecular weight of 230.73 g/mol.

Based on its molecular formula C12H19ClO2, Endo-(1s)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl chloroacetate contains a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 230.73 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC12H19ClO2
Molecular Weight230.73 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1978
Halogen ContentCl-containing

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