127204-71-1

Basic information

• Product Name: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE
• Synonyms: BUTTPARK 9\02-25;IMIDAZO[2,1-B]BENZOTHIAZOLE-3-CARBOXALDEHYDE, 2-PHENYL-;2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBALDEHYDE;2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE
• CAS NO: 127204-71-1
• Molecular Formula: C₁₆H₁₀N₂OS
• Molecular Weight: 278.33
• Mol File: 127204-71-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE(127204-71-1)
• EPA Substance Registry System: 2-PHENYL-BENZO[D]IMIDAZO[2,1-B]THIAZOLE-3-CARBOXALDEHYDE(127204-71-1)

Safety Data

• Hazardous Substances Data: 127204-71-1(Hazardous Substances Data)

Upstream product

• 70-11-1 α-bromoacetophenone 
• 136-95-8 2-amino-benzthiazole 
• 17833-07-7 2-phenylimidazo[2,1-b]benzothiazole 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 5005-14-1 N-(benzo[d]thiazol-2-yl)benzamide 
• 37654-58-3 3-bromo-2-phenylbenzo[d]imidazo[2,1-b]thiazole 
• 1268167-83-4 3-iodo-2-phenylbenzo[d]imidazo[2,1-b]thiazole 
• 127204-75-5 (-)-ethyl 3-hydroxy-3-<2-phenylimidazo<2,1-b>benzothiazol-3-yl>propionate 
• 127204-75-5 (+)-ethyl 3-hydroxy-3-<2-phenylimidazo<2,1-b>benzothiazol-3-yl>propionate 
• 127204-75-5 ethyl 3-hydroxy-3-<2-phenylimidazo<2,1-b>benzothiazol-3-yl>propionate 

Relevant articles and documents

Metal-free oxidative decarbonylative halogenation of fused imidazoles

An efficient strategy has been developed for the deformylative halogenation of carbaldehyde imidazo-fused heterocycles in the presence of TBHP controlled by temperature. A convenient and sequential functionalization (C8 to C3) portrays the synthetic utility of the current method.N-Heterocycle benzamide products were also observedviathe ring opening of imidazopyridines through the cleavage of C-C bond at high temperatures. Features of this method include temperature-controlled excellent regioselectivity, mild conditions and functional group tolerance.

Imidazo[2,1-b]benzothiazoles, II. Synthesis and antiinflammatory activity of some imidazo[2,1-b]benzothiazoles

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