42216-95-5

Usage

InChI:InChI=1/C9H19BrO3/c1-5-11-9(8(4)10,12-6-2)13-7-3/h8H,5-7H2,1-4H3

Upstream product

• 115-80-0 Triethyl orthopropionate 

Downstream Products

• 21504-43-8 1,1-di-ethoxyprop-1-ene 
• 42216-96-6 triethyl orthoacrylate 
• 42217-00-5 3,3,3-triethoxypropyne 
• 118451-60-8 ethyl 4-methylcyclohexa-1,4-dienecarboxylate 
• 118451-58-4 4,6-Dimethyl-cyclohexa-1,4-dienecarboxylic acid ethyl ester 
• 118451-56-2 4,6,6-Trimethyl-cyclohexa-1,4-dienecarboxylic acid ethyl ester 
• 118451-59-5 ethyl 4,5-dimethylcyclohexa-1,4-dienecarboxylate 
• 660417-39-0 2-(1-bromo-ethyl)-5-(3-chloro-phenyl)-[1,3,4]oxadiazole 
• 1349191-55-4 (S)-ethyl-5-(benzylamino)-6-phenyl-hex-2-ynoate 
• 657424-54-9 2-(1-bromo-ethyl)-5-(2-fluoro-5-methyl-phenyl)-[1,3,4]oxadiazole 
• 657424-50-5 2-(1-bromo-ethyl)-5-(5-chloro-2-fluoro-phenyl)-[1,3,4]oxadiazole 

Relevant academic research and scientific papers

Practical synthesis of functionalized terminal alkynes, 3,3,3-triethoxypropyne and ketal protected prop-2-ynones

Practical and economical synthesis of synthetically valuable 3,3,3-triethoxypropyne, ketal protected phenyl and methyl substituents prop-2-ynones is described. Bromination and subsequent 18-crown-6 catalyzed elimination of triethylorthoacrylate and ketal

Polymerizable bicyclic orthoester compounds

Certain new derivatives of 2,6,7-trioxabicyclo[2,2,2]octane are found to undergo cationic ring-opening polymerization with positive expansion in volume or with no substantial change in volume, in contrast with known polymerizable compounds such as epoxides which present considerable shrinkage in volume on polymerization. These new bicyclic orthoester compounds can be prepared in a facile way known per se.