73739-68-1

Basic information

• Product Name: acide methoxy-5 methylene-2 dimethyl-6,6 cyclohexane acetique
• CAS NO: 73739-68-1
• Molecular Weight: 212.289
• Mol File: 73739-68-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: acide methoxy-5 methylene-2 dimethyl-6,6 cyclohexane acetique(CAS DataBase Reference)
• NIST Chemistry Reference: acide methoxy-5 methylene-2 dimethyl-6,6 cyclohexane acetique(73739-68-1)
• EPA Substance Registry System: acide methoxy-5 methylene-2 dimethyl-6,6 cyclohexane acetique(73739-68-1)

Safety Data

• Hazardous Substances Data: 73739-68-1(Hazardous Substances Data)

Upstream product

• 18871-66-4 N,N-dimethylacetamide dimethyl acetal 
• 73739-63-6 hydroxymethyl-1 methoxy-4 dimethyl-3,3 cyclohexene-1 
• 73739-64-7 (methoxy-4 dimethyl-3,3 cyclohexene-1 ylmethyl) vinylether 
• 78-39-7 Triethyl orthoacetate 
• 73739-62-5 formyl-1 methoxy-4 dimethyl-3,3 cyclohexene-1 
• 73739-61-4 1,1,3,7,7-pentamethoxy-2,2-dimethyl-heptane 
• 4454-02-8 1,1,5,5-tetramethoxy-pentane 
• 4454-05-1 2-methoxy-3,4-dihydro-2H-pyran 

Relevant articles and documents

Une voie d'acces aux alcoxy-5 trimethyl-4,4,7a hexahydro-3aα,4,5,6,7,7aα (3H)-benzofurannones-2

Starting from 2-methoxy (or ethoxy)-3,4-dihydro-2H-pyran, a series of four reactions allows to obtain a good yield of two 4-alcoxy-3,3-dimethyl-1-hydroxymethyl cyclohexenes which are converted to methylenecyclohexylacetic acids by different or sigmatropic reactions.These acids are cyclized at room temperature with concentrated sulfuric acid into bicyclic γ-lactones having a cis-junction.The stereospecificity of this reaction and the stability of the isomers obtained are discussed.