321922-24-1

Basic information

• Product Name: Phenol, 3-ethenyl-4-(1-methylethoxy)-
• CAS NO: 321922-24-1
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 321922-24-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenol, 3-ethenyl-4-(1-methylethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-ethenyl-4-(1-methylethoxy)-(321922-24-1)
• EPA Substance Registry System: Phenol, 3-ethenyl-4-(1-methylethoxy)-(321922-24-1)

Safety Data

• Hazardous Substances Data: 321922-24-1(Hazardous Substances Data)

Upstream product

• 321922-22-9 2,2-dimethyl-propionic acid 4-isopropoxy-3-vinyl-phenyl ester 
• 1371631-32-1 3-formyl-4-(propan-2-yloxy)phenyl benzoate 
• 890127-49-8 3-ethenyl-4-(propan-2-yloxy)phenyl benzoate 
• 147067-92-3 2-hydroxy-5-benzoyloxybenzaldehyde 
• 137871-27-3 2,5-bis-benzoyloxy-benzaldehyde 
• 75-30-9 2-iodo-propane 
• 1194-98-5 2,5-Dihydroxybenzaldehyde 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 321922-23-0 2,2-dimethyl-propionic acid 3-formyl-4-isopropoxy-phenyl ester 
• 178547-40-5 2-hydroxy-5-(t-butylcarbonyloxy)benzaldehyde 

Downstream Products

• 607364-51-2 5-(4-chlorobutoxy)-2-isopropoxystyrene 
• 1208610-03-0 di-tert-butyl 2,2'-(6-(4-isopropoxy-3-vinylphenoxy)-1,3,5-triazine-2,4-diyl)bis(azanediyl)-bis(ethane-2,1-diyl)dicarbamate 
• 1208610-04-1 2,4-diamino-6-(4-isopropoxy-3-vinylphenoxy)-1,3,5-triazine 
• 1371631-33-2 C₁₇H₂₈O₅Si 
• 1224465-59-1 2-(4-isopropoxy-3-vinylphenoxy)acetic acid 
• 952525-54-1 C₂₁H₃₅NO₆Si 
• 607364-52-3 1-[4-(4-isopropoxy-3-vinyl-phenoxy)-butyl]-1H-imidazole 

Relevant articles and documents

First elaboration of an olefin metathesis catalytic membrane by grafting a Hoveyda–Grubbs precatalyst on zirconia membranes

This study is aimed at developing an innovative concept for the preparation of an olefin metathesis catalytic membrane. This goal was achieved by grafting a Grubbs II precatalyst on a zirconia membrane generating a tailor-made Hoveyda–Grubbs precatalyst o

Preparation of some nitrogen-containing 2,5-dialkoxystyrene derivatives

The synthesis of 2,5-dialkoxystyrene derivatives starting from 2,5-dihydroxybenzaldehyde is described. The key steps in the synthesis are the alkylation of the phenolic hydroxyl groups and subsequent Wittig olefination of the aldehyde moiety. The ether side-chains of the products display several nitrogen-containing functional groups, including phthalimido, tertbutoxycarbonylamino, cyano and aminotriazines.

A soluble polymer-bound ruthenium carbene complex: A robust and reusable catalyst for ring-closing olefin metathesis

Poly(ethylene glycol)(PEG)-bound Ru carbene complex 3, prepared from functionalized styrene 1 and Grubbs catalyst 2, exhibits remarkable stability and catalyzes the ring-closing metathesis of a variety of α,ω-dienes, and leads to the formation of five-, s