16695-87-7

Basic information

• Product Name: 3-Cyclohexene-1-carboxylic acid, 1,4-dimethyl-
• CAS NO: 16695-87-7
• Molecular Formula: C9H14O2
• Molecular Weight: 154.209
• Mol File: 16695-87-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-Cyclohexene-1-carboxylic acid, 1,4-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclohexene-1-carboxylic acid, 1,4-dimethyl-(16695-87-7)
• EPA Substance Registry System: 3-Cyclohexene-1-carboxylic acid, 1,4-dimethyl-(16695-87-7)

Safety Data

• Hazardous Substances Data: 16695-87-7(Hazardous Substances Data)

Upstream product

• 79-41-4 poly(methacrylic acid) 
• 78-79-5 isoprene 
• 139404-50-5 (1S,4R)-2-((R)-1,4-Dimethyl-cyclohex-3-enecarbonyl)-4,7,7-trimethyl-2-aza-bicyclo[2.2.1]heptan-3-one 
• 139278-33-4 (1R,4S)-3-Methacryloyl-1,7,7-trimethyl-3-azabicyclo<2.2.1>heptan-2-one 
• 24326-88-3 (1S)-4,7,7-trimethyl-2-azabicyclo<2.2.1>heptan-3-one 
• 58911-05-0 1,4-Dimethyl-3-cyclohexen-1-carbonsaeure-methylester 
• 50552-19-7 ethyl-1,4-dimethylcyclohexene-4-carboxylate 
• 80-62-6 methacrylic acid methyl ester 
• 97-63-2 methyl methacrylate 

Downstream Products

• 1427276-87-6 2-(1,4-dimethylcyclohex-3-enyl)-1H-indole 
• 1427276-85-4 1,4-dimethyl-N-m-tolylcyclohex-3-enecarboxamide 
• 1427276-84-3 1,4-dimethyl-N-o-tolylcyclohex-3-enecarboxamide 
• 50552-16-4 1,4-Dimethyl-4-nitrosooxymethyl-cyclohexene 
• 933-44-8 1,4-dimethyl-cyclohex-3-enecarbaldehyde 
• 24097-66-3 1,4-Dimethyl-cyclohexanecarboperoxoic acid tert-butyl ester 
• 24097-65-2 1,4-Dimethyl-cyclohexanecarboperoxoic acid tert-butyl ester 
• 24097-72-1 trans-1,4-Dimethyl-cyclohexancarbonsaeurechlorid 
• 24097-73-2 cis-1,4-Dimethyl-cyclohexancarbonsaeurechlorid 
• 24097-70-9 1,4c-dimethyl-cyclohexane-r-carboxylic acid 
• 24097-71-0 1,4t-dimethyl-cyclohexane-r-carboxylic acid 
• 107688-45-9 N-benzyl-N-(1,4-dimethyl-3-cyclohexenyl)methylamine hydrochloride 
• 107765-73-1 N-benzyl-2,5-dimethyl-7-azabicyclo<3.3.1>non-2-ene 
• 78142-69-5 cis-1,4-dimethyl-4-bromo-1-benzoylcyclohexane 

Relevant articles and documents

Diels-Alder reactions in pyridinium based ionic liquids

Diels-Alder reactions have been investigated in pyridinium based ionic liquids. These solvents are found to be more effective compared to the organic solvent studied, in enhancing the reaction rate and product yields. Recycled ionic liquids also gave exce

Toward the Development of a General Chiral Auxiliary. 1. Preparation of a New Class of Camphor Lactam Imides and Their Application to the Construction of Quaternary Centers via Diels-Alder Cycloaddition

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First Synthesis of rac-Homofenchone (1,4,4-Trimethylbicyclooctan-3-one)

The rac-homofenchone (2), which was previously unknown, is prepared starting from the cyclohexenecarboxylate 4 via the bicyclooctene 13 by two independent routes.The key steps are either the intramolecular acylation of a C=C bond in 9 induced by trifluoroacetic acid anhydride, or the BF3-catalyzed decomposition of the diazomethyl ketone 15.From 13 a direct path leads to homofenchone (2), the NMR spectra of which were fully assigned.