869542-39-2

Basic information

• Product Name: phenyl[2-[tris(1-methylethyl)silyl]-1,3-oxazol-5-yl]methanol
• Synonyms: phenyl[2-[tris(1-methylethyl)silyl]-1,3-oxazol-5-yl]methanol
• CAS NO: 869542-39-2
• Molecular Weight: 331.53
• Mol File: 869542-39-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: phenyl[2-[tris(1-methylethyl)silyl]-1,3-oxazol-5-yl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl[2-[tris(1-methylethyl)silyl]-1,3-oxazol-5-yl]methanol(869542-39-2)
• EPA Substance Registry System: phenyl[2-[tris(1-methylethyl)silyl]-1,3-oxazol-5-yl]methanol(869542-39-2)

Safety Data

• Hazardous Substances Data: 869542-39-2(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 433332-27-5 2-[tris(propan-2-yl)silyl]-1,3-oxazole 
• 869542-45-0 2-[tris(1-methylethyl)silyl]-1,3-oxazole-5-carbaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 108-86-1 bromobenzene 

Downstream Products

• 945017-34-5 5-[azido(phenyl)methyl]-2-(triisopropylsilyl)-1,3-oxazole 

Relevant articles and documents

Investigation of the hydroxyl directing effect on the Paternò–Büchi reaction on 5-(2-triisopropylsilyloxazolyl)methanol derivatives

The photochemical coupling of 5-oxazoylmethanol derivatives with benzophenone and benzaldehyde showed that the hydroxyl directing effect in the Paternò–Büchi reaction described in the case of allylic alcohols and furylmethanol derivatives can also be pres

A convenient oxazole C-2 protecting group: The synthesis of 4- and 5-substituted oxazoles via metalation of 2-triisopropylsilyloxazoles

Metalation of oxazoles at the 4 and 5 position was achieved after regioselective C-2 silyl protection. Removal of the protecting group was then accomplished under mild conditions allowing for a straightforward preparation of C-5 monosubstituted and C-4,5