1016928-35-0

Basic information

• Product Name: 1,3-bis(4,5-dihydrothiazol-2-yl)benzene
• Synonyms: 1,3-bis(4,5-dihydrothiazol-2-yl)benzene
• CAS NO: 1016928-35-0
• Molecular Weight: 248.373
• Mol File: 1016928-35-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3-bis(4,5-dihydrothiazol-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis(4,5-dihydrothiazol-2-yl)benzene(1016928-35-0)
• EPA Substance Registry System: 1,3-bis(4,5-dihydrothiazol-2-yl)benzene(1016928-35-0)

Safety Data

• Hazardous Substances Data: 1016928-35-0(Hazardous Substances Data)

Upstream product

• 626-17-5 benzene-1,3-dicarbonitrile 
• 60-23-1 Cysteamine 
• 156-57-0 2-mercaptoethylamine hydrochloride 
• 1370477-93-2 3-(4,5-dihydrothiazol-2-yl)benzonitrile 

Downstream Products

• 13816-22-3 1,3-di(thiazol-2-yl)benzene 

Relevant articles and documents

1,3-Dibromo-5,5-dimethylhydantoin as an efficient homogeneous catalyst for the synthesis of 2-arylthiazolines and 2-arylimidazolines

A simple, facile, and efficient procedure for the synthesis of 2-arylthizolines and 2-arylimidazolines has been developed by the simple condensation of nitriles with 2-aminoethanethiol or ethylenediamine catalyzed by 1,3-dibromo-5,5-dimethylhydantoin under solvent-free conditions. Selective preparation of bisthiozolines and monoimidazolines from dinitriles and also selective conversion of arylnitriles to their corresponding 2-arylthiazolines or imidazolines in the presence of alkylnitriles can be considered as considerable advantages of this method.

DDQ-induced dehydrogenation of heterocycles for c-c double bond formation: Synthesis of 2-thiazoles and 2-oxazoles

Strong as an Ox: 2-Thiazoles and 2-oxazoles are formed by oxidation of 2-thiazolines and 2-oxazolines without requiring substituents at the C4 and C5 positions. DDQ plays an important role as the oxidant in this transformation and metal is unnecessary. This general procedure shows good functional group tolerance and provides a wide variety of 2-thiazoles and 2-oxazoles in moderate to excellent yields.