1341125-81-2

Basic information

• Product Name: 1-[3-hydroxy-3-(4-isopropoxyphenyl)prop-1-ynyl]cyclopentanol
• CAS NO: 1341125-81-2
• Molecular Weight: 274.36
• Mol File: 1341125-81-2.mol

Chemical Properties

• CAS DataBase Reference: 1-[3-hydroxy-3-(4-isopropoxyphenyl)prop-1-ynyl]cyclopentanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[3-hydroxy-3-(4-isopropoxyphenyl)prop-1-ynyl]cyclopentanol(1341125-81-2)
• EPA Substance Registry System: 1-[3-hydroxy-3-(4-isopropoxyphenyl)prop-1-ynyl]cyclopentanol(1341125-81-2)

Safety Data

• Hazardous Substances Data: 1341125-81-2(Hazardous Substances Data)

Upstream product

• 17356-19-3 1-ethynylcyclopentanol 
• 18962-05-5 4-isopropoxybenzaldehyde 

Downstream Products

• 1341125-98-1 4-butylidene-2-(4-isopropoxyphenyl)-1-oxaspiro[4.4]non-2-ene 
• 1341125-99-2 1-{1-[2-(4-isopropoxyphenyl)ethyl]pentyl}cyclopentanol 
• 1341126-00-8 4-hexylidene-2-(4-isopropoxyphenyl)-1-oxaspiro[4.4]non-2-ene 
• 1341126-01-9 2-(4-isopropoxyphenyl)-4-methylene-1-oxaspiro[4.4]non-2-ene 
• 1341126-03-1 4-butylidene-3-fluoro-2-(4-isopropoxyphenyl)-1-oxaspiro[4.4]non-2-ene 
• 1341126-04-2 4-butylidene-3-chloro-2-(4-isopropoxyphenyl)-1-oxaspiro[4.4]non-2-ene 
• 1341126-05-3 4-butylidene-2-(4-isopropoxyphenyl)-3-phenyl-1-oxaspiro[4.4]non-2-ene 
• 1341125-82-3 3-(1-hydroxycyclopentyl)-1-(4-isopropoxyphenyl)propynone 
• 1341125-83-4 2-(4-isopropoxyphenyl)-1-oxaspiro[4.4]non-2-en-4-one 
• 1341125-97-0 2-(4-hydroxyphenyl)-3-phenyl-1-oxaspiro[4.4]non-2-en-4-one 
• 1341125-96-9 2-(4-hydroxyphenyl)-4-oxo-1-oxaspiro[4.4]non-2-ene-3-carboxylic acid amide 
• 1341125-95-8 2-(4-hydroxyphenyl)-4-oxo-1-oxaspiro[4.4]non-2-ene-3-carbonitrile 
• 1341125-94-7 2-(4-hydroxyphenyl)-3-iodo-1-oxaspiro[4.4]non-2-en-4-one 
• 1341125-93-6 3-bromo-2-(4-hydroxyphenyl)-1-oxaspiro[4.4]non-2-en-4-one 

Relevant articles and documents

Limno-CP: A natural-product-inspired 5-aryl-3(2 H)-furanone as scaffold for a library of α-modified enones

A library of 5-aryl-3(2H)-furanones that are modified in the α-position of the α,β-unsaturated carbonyl system was prepared via simple one- to three-step transformations from one common scaffold. The 13C NMR characterization of the enone system showed a strong influence of the α-substituents, especially on the shifts of the α- and β-carbon atoms. Probing the addition chemistry of nucleophiles versus our α-modified enones, a 1,2-addition-elimination- was found, but no 1,4-addition. Georg Thieme Verlag Stuttgart. New York.