1727-76-0 Usage
Uses
Used in Pharmaceutical and Fine Chemicals Production:
2,3,3-trimethylcyclopent-1-enylacetonitrile is utilized as a building block and synthetic intermediate for the production of pharmaceuticals and other fine chemicals. Its unique structure and reactivity make it a key component in the synthesis of complex organic molecules.
Used in Fragrance Industry:
In the fragrance industry, 2,3,3-trimethylcyclopent-1-enylacetonitrile is used as a fragrance ingredient due to its strong and distinctive odor. It contributes to the creation of various scents in perfumes and personal care products, enhancing their appeal to consumers.
Used in Flavor Manufacturing:
2,3,3-trimethylcyclopent-1-enylacetonitrile also finds application in the manufacturing of flavors, where it is employed to impart specific tastes and aromas to food and beverage products, adding to their sensory qualities.
Used in Agrochemicals Production:
2,3,3-trimethylcyclopent-1-enylacetonitrile is used in the production of agrochemicals, where it serves as a key intermediate in the synthesis of various agricultural products, such as pesticides and herbicides, contributing to the development of effective solutions for crop protection.
Used in Industrial Product Manufacturing:
2,3,3-trimethylcyclopent-1-enylacetonitrile has a wide range of applications in the manufacturing of other industrial products, where its chemical properties are harnessed to create a variety of goods that serve different purposes and industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1727-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1727-76:
(6*1)+(5*7)+(4*2)+(3*7)+(2*7)+(1*6)=90
90 % 10 = 0
So 1727-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N/c1-8-9(5-7-11)4-6-10(8,2)3/h4-6H2,1-3H3
1727-76-0Relevant academic research and scientific papers
Beckmann Rearrangement of Oximes Catalyzed with Tetrabutylammonium Perrhenate and Trifluoromethanesulfonic Acid
Kusama, Hiroyuki,Yamashita, Yuko,Narasaka, Koichi
, p. 373 - 377 (2007/10/02)
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.
NOVEL PRODUCTS FROM BECKMANN FRAGMENTATION OF CAMPHOR OXIME IN POLYPHOSPHORIC ACID
Hill, Richard K.,McKinnie, B. Gary,Conley, Robert T.,Darby, Paul S.,Halbeek, Herman van,Holt, Elizabeth M.
, p. 3405 - 3412 (2007/10/02)
Heating camphor oxime with PPA affords, besides the known fragmentation products isoaminocamphor (4) and β-campholenonitrile (13), four isomeric ketones C10H14O resulting from intramolecular acylation of the intermediate α-campholenonitrile (3).The ketones have been identified as 5-ketocamphene (6), 6-ketocamphene (8), tricyclenone (9), and endo-2,4-dimethylbicyclooct-2-ene-7-one (14).The latter results from a novel ring expansion, probably by way of a protonated cyclopropane.
INSECT GROWTH REGULATORS. PART XV. SYNTHESES OF JUVENOIDS WITH THE 2,3,3-TRIMETHYL-1-CYCLOPENTENE SYSTEM
Wawrzenczyk, Czeslaw
, p. 135 - 147 (2007/10/02)
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.
