53907-70-3

Basic information

• Product Name: 2,2,4-Trimethyl-4-penten-1-ol
• Synonyms: 2,2,4-Trimethyl-4-penten-1-ol
• CAS NO: 53907-70-3
• Molecular Formula: C₈H₁₆O
• Molecular Weight: 128.21
• Mol File: 53907-70-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2,4-Trimethyl-4-penten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,4-Trimethyl-4-penten-1-ol(53907-70-3)
• EPA Substance Registry System: 2,2,4-Trimethyl-4-penten-1-ol(53907-70-3)

Safety Data

• Hazardous Substances Data: 53907-70-3(Hazardous Substances Data)

Upstream product

• 39482-50-3 2,2,4-trimethylpent-4-enal 
• 56001-56-0 2,2,4-trimethyl-4-pentenoic acid 
• 71672-41-8 methyl 2,2,4-trimethylpent-4-enoate 

Downstream Products

• 155934-08-0 (E)-1-acetoxy-9-(4-methoxybenzyloxy)-6,6,8-trimethyl-2-nonane 
• 155934-02-4 ethyl (E)-7-(4-methoxybenzyloxy)-4,4,6-trimethyl-2-heptanoate 
• 155934-06-8 methyl (E)-9-(4-methoxybenzyloxy)-6,6,8-trimethyl-2-noneoate 
• 155934-03-5 ethyl 7-(4-methoxybenzyloxy)-4,4,6-trimethylheptanoate 
• 155933-99-6 5-(4-methoxybenzyl)-2,2,4-trimethyl-1-dimethylthexylsilyloxypentane 
• 155934-07-9 (E)-9-(4-methoxybenzyloxy)-6,6,8-trimethyl-2-nonen-1-ol 
• 155934-05-7 7-(4-Methoxy-benzyloxy)-4,4,6-trimethyl-heptanal 
• 155934-01-3 5-(4-Methoxy-benzyloxy)-2,2,4-trimethyl-pentanal 
• 155934-04-6 ethyl 7-(4-methoxybenzyloxy)-4,4,6-trimethyl-1-heptanol 
• 155934-00-2 5-(4-methoxybenzyloxy)-2,2,4-trimethyl-1-pentanol 
• 691900-19-3 N-ethynyl-4-methyl-N-(2,2,4-trimethyl-pent-4-enyl)-benzenesulfonamide 
• 114445-41-9 4-methyl-N-(2,2,4-trimethyl-pent-4-enyl)-benzenesulfonamide 

Relevant articles and documents

Rhodium-Catalyzed Cyclization of O,ω-Unsaturated Alkoxyamines: Formation of Oxygen-Containing Heterocycles

O,ω-Unsaturated N-tosyl alkoxyamines undergo unexpected RhIII-catalyzed intramolecular cyclization by oxyamination to produce oxygen-containing heterocycles. Mechanistic studies show that an aziridine intermediate seems to be responsible for the formation of the heterocycles, possibly via a RhV species.

Intramolecular Olefinic Aldehyde Prins Reactions for the Construction of Five-Membered Rings

Four catalysts (Me2AlCl SnCl4 > EtAlCl2 > Et2AlCl) for the cyclization of olefinic aldehydes by an internal Prins mechanism have been compared by using systems that afford five-membered rings by type I and type II ene processes.Stannic chloride and Me