67175-80-8

Basic information

• Product Name: 1-methoxy-4-(2-hydroxyethyl)-cyclohexa-1,4-diene
• Synonyms: 1-methoxy-4-(2-hydroxyethyl)-cyclohexa-1,4-diene
• CAS NO: 67175-80-8
• Molecular Weight: 154.209
• Mol File: 67175-80-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-methoxy-4-(2-hydroxyethyl)-cyclohexa-1,4-diene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methoxy-4-(2-hydroxyethyl)-cyclohexa-1,4-diene(67175-80-8)
• EPA Substance Registry System: 1-methoxy-4-(2-hydroxyethyl)-cyclohexa-1,4-diene(67175-80-8)

Safety Data

• Hazardous Substances Data: 67175-80-8(Hazardous Substances Data)

Upstream product

• 702-23-8 2-(4-Methoxyphenyl)ethanol 
• 7439-93-2 lithium 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 32863-01-7 4-(2-hydroxyethyl)cyclohexan-1-one 
• 1616766-78-9 2-(4-oxocyclohexyl)ethyl 4-chlorobenzoate 
• 1616766-79-0 (R)-2-(4-oxocyclohex-2-en-1-yl)ethyl 4-chlorobenzoate 
• 32863-02-8 2-(4-oxocyclohexyl)ethyl acetate 
• 628731-60-2 4-(2-(benzyloxy)ethyl)cyclohexan-1-one 

Relevant articles and documents

Synthesis of cationic 1-substituted-dicarbonyl(η5-4- methoxycyclohexadienyl)-(triphenylphosphine)iron complexes

Cationic 1-substituted-dicarbonyl(π5-4-methoxycyclohexadienyl)- (triphenylphosphine)iron complexes 10 form a new class of highly functionalised iron complexes which have never been described. They were obtained from neutral 1-substituted (πsup

Reductive cyclization strategy for construction of the highly oxygenated CD ring system of aconitine

The synthesis of a CD ring analogue of aconitine is described. The SmI2-mediated reductive cyclization of an α,β-epoxyketone with a pendant formyl group allowed for stereocontrolled construction of the bicyclo[3.2.1]octane framework. Further ox

From meiogynin A to the synthesis of dual inhibitors of Bcl-xL and Mcl-1 anti-apoptotic proteins

The synthesis of one of the most potent dual inhibitors of the anti-apoptotic proteins Bcl-xL and Mcl-1 is reported. This analogue of a natural sesquiterpenoid dimer meiogynin A was elaborated by a convergent asymmetric synthesis with 36% yield in ten steps. the Partner Organisations 2014.