1315510-22-5

Basic information

• Product Name: dimethyl 2,2'-diphenyl-bis-5,5'-thiazole-4,4'-dicarboxylate
• Synonyms: dimethyl 2,2'-diphenyl-bis-5,5'-thiazole-4,4'-dicarboxylate
• CAS NO: 1315510-22-5
• Molecular Weight: 436.512
• Mol File: 1315510-22-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: dimethyl 2,2'-diphenyl-bis-5,5'-thiazole-4,4'-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 2,2'-diphenyl-bis-5,5'-thiazole-4,4'-dicarboxylate(1315510-22-5)
• EPA Substance Registry System: dimethyl 2,2'-diphenyl-bis-5,5'-thiazole-4,4'-dicarboxylate(1315510-22-5)

Safety Data

• Hazardous Substances Data: 1315510-22-5(Hazardous Substances Data)

Upstream product

• 1038-95-5 Tri(p-tolyl)phosphine 
• 7113-02-2 2-phenyl-1,3-thiazole-4-carboxylic acid methyl ester 
• 6224-63-1 tri(m-tolyl)phosphine 
• 603-35-0 triphenylphosphine 
• 13406-29-6 tris(para-trifluoromethyl)phenyl phosphine 
• 1159-54-2 tri(4-chlorophenyl)phosphine 
• 18437-78-0 P(p-C₆H₄F)3 
• 855-38-9 P(p-CH₃OC₆H₄)3 
• 932-90-1 Benzaldoxime 
• 100-47-0 benzonitrile 
• 100-52-7 benzaldehyde 
• 3113-46-0 2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid methyl ester 
• 62096-93-9 2-phenyl-4,5-dihydrothiazole-4-carboxylic acid 
• 97-63-2 methyl methacrylate 

Relevant articles and documents

Aryl-aryl coupling via palladium-catalyzed C-P/C-H bond cleavage

The first example of aryl-aryl coupling through palladium-catalyzed C-P/C-H bond cleavage with good functional group tolerance is disclosed. This work demonstrates the phosphines could be used as coupling partners in palladium-catalyzed aryl-aryl coupling

Palladium(II)-catalyzed oxidative Heck coupling of thiazole-4-carboxylates

Oxidative Heck coupling of thiazole-4-carboxylates via palladium(II)- catalyzed C-H bond activation has been achieved in moderate to good yields. No ligand, and no acidic additive were used in the reaction. The results showed that this protocol tolerated