N-(tert-butyl)-3-(6-chloroimidazo[2,1-b]thiazol-5-yl)acrylamide CAS 746606-50-8

Purity 97%+In StockPharmaceutical Standards
CAS No.746606-50-8
Molecular FormulaC12H14ClN3OS
Molecular Weight283.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(tert-butyl)-3-(6-chloroimidazo[2,1-b]thiazol-5-yl)acrylamide CAS 746606-50-8 chemical structure

Description

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

CATO supplies N-(tert-butyl)-3-(6-chloroimidazo[2,1-b]thiazol-5-yl)acrylamide (CAS 746606-50-8), a certified reference material (molecular formula C12H14ClN3OS, MW 283.78 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H14ClN3OS, N-(tert-butyl)-3-(6-chloroimidazo[2,1-b]thiazol-5-yl)acrylamide contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 283.78 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

As a certified reference material (CRM), N-(tert-butyl)-3-(6-chloroimidazo[2,1-b]thiazol-5-yl)acrylamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC12H14ClN3OS
Molecular Weight283.78 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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