52557-98-9

Usage

Uses

Used in Pharmaceutical Industry:
3,3-dimethylbicyclo[2.2.1]heptane-2-carboxylic acid is used as a pharmaceutical precursor for the synthesis of various medicinal compounds. Its unique bicyclic structure and reactivity make it a valuable building block in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, 3,3-dimethylbicyclo[2.2.1]heptane-2-carboxylic acid serves as a versatile precursor. Its complex structure allows for the creation of a wide range of organic compounds, making it a useful component in the synthesis of various chemical products.
Used in Chemical Research:
3,3-dimethylbicyclo[2.2.1]heptane-2-carboxylic acid is used as a subject of study in chemical research. Its unique structure and potential reactivity offer opportunities for exploration in various chemical processes and reactions, contributing to the advancement of chemical knowledge and technology.

InChI:InChI=1/C10H16O2/c1-10(2)7-4-3-6(5-7)8(10)9(11)12/h6-8H,3-5H2,1-2H3,(H,11,12)

Upstream product

• 79-92-5 camphene 
• 3350-78-5 3,3-Dimethylacryloyl chloride 
• 84473-81-4 6,6-dimethylbicyclo(2.2.1)hept-2-ene-5-carbonyl chloride 
• 77-73-6 bi(cyclopentadiene) 
• 875-03-6 Camphene epoxide 

Relevant academic research and scientific papers

A versatile cobalt(II)-Schiff base catalyzed oxidation of organic substrates with dioxygen: Scope and mechanism

Cobalt(II) complex 1a-f derived from Schiff bases act as efficient catalysts during the oxidation of wide range of organic substrates(e.g. alkenes, alcohols, benzylic compounds and aliphatic hydrocarbons) with dioxygen in the presence of aliphatic aldehydes or ketones or ketoesters. EPR studies on 1a-f complexes suggest that the aliphatic carbonyl compounds promote the formation of a cobalt(II)-superoxo species responsible for the oxidation of organic compounds. These studies also demonstrate the role of ligands on cobalt in controlling the chemoselectivity of these oxidations. A plausible mechanistic rational is also provided for these oxidations.

Cobalt catalyzed oxidation of cyclic alkenes with molecular oxygen: Allylic oxidation versus double bond attack

Cobalt (II) Schiff's base complex 1 and 2 exhibit a remarkable chemoselectivity during oxidation of cyclic alkenes with molecular oxygen in the presence of 2-methylpropanal. Catalyst 1 encourages the oxidation of double bond to give epoxide as the major product whereas catalyst 2 promotes mainly the allylic oxidation leading to allylic alcohols or enones.

Traction drive fluid, process for producing the same and bicyclo octane compound

A traction drive fluid composition comprising a hydrocarbon having a bicyclo octane skeleton, such as a bicyclo(3,2,1) octane skeleton, a bicyclo(2,2,2)octane skeleton or a bicyclo(3,3,0)octane skeleton. The traction drive fluid has a low viscosity and has a high traction coefficient over a wide temperature range.

A Simple One-pot Method for Conversion of Terminal Alkenes into Carboxylic Acids via Hydroboration

Hydroboration of terminal alkenes with NaBH4/CH3COOH followed by oxidation with aqueous chromic acids in the presence of t-butanol gives the corresponding carboxylic acids in moderate to good yields (50-75percent).

Chromic Acid Oxidation of Some Oxiranes

Oxiranes derived from some alkenes, with olefinic bonds present in different stereoelectronic environments, have been treated with Cr(VI)-reagents.The major products obtained have been identified and their formation rationalized.In some cases, the method becomes synthetically useful for C-C bond cleavage.