26585-74-0

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
(R)-2,2,3-Trimethylcyclopent-3-ene-1-acetonitrile is utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its role in these industries is crucial for the development of new drugs and agricultural products, contributing to advancements in healthcare and agriculture.
Used in Fragrance Industry:
In the fragrance industry, (R)-2,2,3-Trimethylcyclopent-3-ene-1-acetonitrile is employed as an ingredient in perfumes and other personal care products. Its distinct odor makes it a valuable addition to the creation of various scents, enhancing the sensory experience of consumers.
Used in Polymer and Dye Production:
(R)-2,2,3-Trimethylcyclopent-3-ene-1-acetonitrile also holds potential in the production of polymers and dyes. Its unique chemical properties allow it to be a versatile building block in the development of new materials with specific characteristics, catering to the needs of various industries.
Safety Precautions:
It is important to handle (R)-2,2,3-Trimethylcyclopent-3-ene-1-acetonitrile with care, as it can be harmful if ingested or inhaled. Additionally, it may cause irritation to the skin and eyes. Proper safety measures should be taken to minimize the risk of exposure and ensure the well-being of those working with (R)-2,2,3-Trimethylcyclopent-3-ene-1-acetonitrile.

InChI:InChI=1/C10H15N/c1-8-4-5-9(6-7-11)10(8,2)3/h4,9H,5-6H2,1-3H3/t9-/m1/s1

Upstream product

• 2792-42-9 (R,R)-camphor oxime 
• 103-72-0 phenyl isothiocyanate 
• 532-55-8 Benzoyl isothiocyanate 
• 736109-58-3 1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 1003311-00-9 (+)-camphor oxime 

Downstream Products

• 23727-15-3 (+)-campholenic aldehyde 
• 91175-74-5 [2-(2,2,3-Trimethylcyclopent-3-enyl)ethyl]-p-toluensulfonat 
• 55730-89-7 5-(2,2,3-trimethyl-cyclopent-3-en-1-yl)-pent-4-en-2-one 
• 91175-73-4 (R)-(+)-ethyl (2,2,3-trimethyl-cyclopent-3-en-1-yl)acetate 
• 52437-39-5 (R)-(+)-2-(2,2,3-trimethyl-cyclopent-3-en-1-yl)ethanol 
• 55730-88-6 5-(2,2,3-trimethyl-cyclopent-3-en-1-yl)-pent-3-en-2-one 

Relevant academic research and scientific papers

Photoinduced Molecular Transformations. Part 119.1 Photochemical Nitrogen Insertion into Bicycloheptanones; the Photochemistry of Oximes of (+)-Fenchone and (+)-Camphor2

The photolysis of the oxime of (+)-fenchone in methanol gave a 1:1 ratio of two isomeric lactams, 1,4,4-trimethyl-2-azabicyclooctan-3-one (13percent) and its previously undescribed isomer, 1,4,4-trimethyl-3-azabicyclooctane-2-one (13percent)

Nitrogen Insertion to Bicycloheptanones; the Photo-Beckmann Rearrangement of Oximes of (+)-Fenchone and (+)-Camphor

The major products of the photolysis of the oximes of two natural bicycloheptanones, (+)-fenchone and (+)-camphor, in methanol are nearly equal amounts of two isomeric lactams arising from the photo-Beckmann rearrangement and the corresponding ring-opened amides.