1225053-32-6

Basic information

• Product Name: 2-phenyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-Thiazole
• Synonyms: 2-phenyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-Thiazole;2-Phenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazole
• CAS NO: 1225053-32-6
• Molecular Formula: C₁₅H₁₈BNO₂S
• Molecular Weight: 287.19
• Mol File: 1225053-32-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-phenyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-Thiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-Thiazole(1225053-32-6)
• EPA Substance Registry System: 2-phenyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-Thiazole(1225053-32-6)

Safety Data

• Hazardous Substances Data: 1225053-32-6(Hazardous Substances Data)

Upstream product

• 1826-11-5 2-phenylthiazole 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 76-09-5 2,3-dimethyl-2,3-butane diol 

Downstream Products

• 1092073-94-3 2-methylsulfanyl-4-(2-phenylthiazol-5-yl)-pyrimidine 
• 3704-40-3 2,5-diphenyl-1,3-thiazole 
• 68004-04-6 5-(4-methoxyphenyl)-2-phenyl-1,3-thiazole 

Relevant articles and documents

ANTIBACTERIAL PYRROLOIMIDAZOLONES

The invention relates to compounds of formula (I)wherein M represents a 5-membered heterocyclic aromatic ring and A is defined in the description. Further, the use of said compounds as antibacterial agents, especially against Gram-negative microorganismsn

A guideline for the arylation of positions 4 and 5 of thiazole via Pd-catalyzed cross-coupling reactions

The arylation of thiazoles in 4- and 5-position was investigated in detail. Suzuki-Miyaura and Stille cross-coupling reactions were tested using thiazoles either as halide or organometal species. The obtained results were critically compared to develop he