1727-76-0

Basic information

• Product Name: 2,3,3-trimethylcyclopent-1-enylacetonitrile
• Synonyms: 2,3,3-trimethylcyclopent-1-enylacetonitrile;2,3,3-Trimethyl-1-cyclopentene-1-acetonitrile
• CAS NO: 1727-76-0
• Molecular Formula: C₁₀H₁₅N
• Molecular Weight: 149.2328
• EINECS: 217-042-2
• Mol File: 1727-76-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 212.6°Cat760mmHg
• Flash Point: 88.6°C
• Appearance: /
• Density: 0.891g/cm³
• Vapor Pressure: 0.172mmHg at 25°C
• Refractive Index: 1.461
• CAS DataBase Reference: 2,3,3-trimethylcyclopent-1-enylacetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,3-trimethylcyclopent-1-enylacetonitrile(1727-76-0)
• EPA Substance Registry System: 2,3,3-trimethylcyclopent-1-enylacetonitrile(1727-76-0)

Safety Data

• Hazardous Substances Data: 1727-76-0(Hazardous Substances Data)

Usage

General Description

2,3,3-trimethylcyclopent-1-enylacetonitrile is a chemical compound that belongs to the class of acetonitriles. It is a clear, colorless liquid with a molecular formula of C10H15N. 2,3,3-trimethylcyclopent-1-enylacetonitrile is commonly used in the synthesis of various organic compounds and can also be used as a building block for the production of pharmaceuticals and other fine chemicals. It is known for its strong odor and is often used as a fragrance ingredient in perfumes and personal care products. Additionally, 2,3,3-trimethylcyclopent-1-enylacetonitrile has applications in the manufacturing of flavors, agrochemicals, and other industrial products.

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

Upstream product

• 2792-42-9 (R,R)-camphor oxime 
• 736109-58-3 1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one 
• 464-48-2 (1S)-camphor 
• 7647-01-0 hydrogenchloride 
• 37939-80-3 1,7,7-trimethyl-bicyclo[2.2.1]heptane-2-one-oxime 
• 1003311-00-9 (+)-camphor oxime 
• 13559-66-5 (+/-)-camphor oxime 
• 75-36-5 acetyl chloride 
• 15373-31-6 α-campholenonitrile 

Downstream Products

• 72445-71-7 N-(β-Campholenyl)-p-chlorbenzylidenimin 
• 72445-79-5 β-Campholenyl-N-(2,3-dichlorphenyl)urethan 
• 72445-69-3 1-(4-Chloro-3-methyl-phenyl)-3-[2-(2,3,3-trimethyl-cyclopent-1-enyl)-ethyl]-urea 
• 72445-68-2 1-(3-Chloro-4-methyl-phenyl)-3-[2-(2,3,3-trimethyl-cyclopent-1-enyl)-ethyl]-urea 
• 72445-78-4 β-Campholenyl-N-(p-chlorphenyl)urethan 
• 72445-84-2 N-(β-Campholenyl)-p-nitrobenzylamin 
• 72445-73-9 N-(β-Campholenyl)-p-nitrobenzylidenimin 
• 72445-66-0 N-(β-Campholenyl)-o-methylphenylharnstoff 
• 72445-65-9 N-(β-Campholenyl)-p-methylphenylharnstoff 
• 72445-67-1 N-(β-Campholenyl)-m-methylphenylharnstoff 
• 72445-63-7 Phenyl-N-(β-campholen)-carbamat 
• 72445-72-8 N-(β-Campholenyl)-p-brombenzylidenimin 
• 72445-83-1 N-(β-Campholenyl)-p-chlorbenzylamin 
• 72445-74-0 N-(β-Campholenyl)-p-methylbenzylidenimin 

Relevant articles and documents

Beckmann Rearrangement of Oximes Catalyzed with Tetrabutylammonium Perrhenate and Trifluoromethanesulfonic Acid

The Beckmann rearrangement of oximes is catalyzed by a combined use of tetrabutylammonium perrhenate (Bu4NReO4) and trifluoromethanesulfonic acid in nitromethane under azeotropic conditions, giving amides in high yield.By employing this catalytic system, amides can be prepared directly from ketones and hydroxylamine hydrochloride.

INSECT GROWTH REGULATORS. PART XV. SYNTHESES OF JUVENOIDS WITH THE 2,3,3-TRIMETHYL-1-CYCLOPENTENE SYSTEM

New analogs of insect juvenile hormone were obtained by a multi-step synthesis starting from β-campholenenitrile (2).The Grignard reaction and the Claisen rearrangement by the orthoacetate method were applied for building and elongating an aliphatic chain.All compounds obtained are characterized by the presence of trans-disubstituted double bonds in the β-position in relation to the cyclopentane ring.