1-(6-Methylthiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl (3,4-dichlorophenyl)carbamate CAS 477859-65-7

Purity 97%+In StockPharmaceutical Standards
CAS No.477859-65-7
Molecular FormulaC14H12Cl2N4O2S
Molecular Weight371.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(6-Methylthiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl (3,4-dichlorophenyl)carbamate CAS 477859-65-7 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution, 1-(6-Methylthiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl (3,4-dichlorophenyl)carbamate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 371.24 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

1-(6-Methylthiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl (3,4-dichlorophenyl)carbamate (CAS 477859-65-7), molecular formula C14H12Cl2N4O2S and molecular weight 371.24 g/mol, is a CATO reference standard with documented purity and traceability.

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 FormulaC14H12Cl2N4O2S
Molecular Weight371.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms1

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