54353-80-9 Usage
Uses
Used in Flavoring Industry:
2-(cyclohex-1-en-1-yl)-2-methylpropanenitrile is utilized as a flavoring agent in the food and beverage industry, particularly for the production of fruit flavors. Its fruity and green notes contribute to the enhancement of the sensory experience of these products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-(cyclohex-1-en-1-yl)-2-methylpropanenitrile serves as an intermediate in the synthesis of various organic compounds and pharmaceuticals, playing a crucial role in the development of new drugs and medicinal products.
Used in Organic Compounds Synthesis:
2-(cyclohex-1-en-1-yl)-2-methylpropanenitrile is also employed as an intermediate in the synthesis of other organic compounds, highlighting its importance in the realm of organic chemistry and its potential applications in various chemical processes.
Safety Precautions:
It is essential to handle 2-(cyclohex-1-en-1-yl)-2-methylpropanenitrile with care due to its potential to irritate the skin, eyes, and respiratory system. It should be used in a well-ventilated area, and appropriate personal protective equipment should be worn to minimize health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 54353-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,5 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54353-80:
(7*5)+(6*4)+(5*3)+(4*5)+(3*3)+(2*8)+(1*0)=119
119 % 10 = 9
So 54353-80-9 is a valid CAS Registry Number.
54353-80-9Relevant academic research and scientific papers
Synthesis of Tertiary Benzylic Nitriles via Nickel-Catalyzed Markovnikov Hydrocyanation of α-Substituted Styrenes
Xing, Yidan,Yu, Rongrong,Fang, Xianjie
, p. 1008 - 1012 (2020/02/04)
The Markovnikov hydrocyanation of α-substituted styrenes enables the synthesis of tertiary benzylic nitriles under nickel catalysis. The Lewis-acid-free transformation features an unprecedented functional groups tolerance, including the-OH and-NH2 groups. A broad range of tertiary benzylic nitriles were obtained in good to excellent yields. In addition, an asymmetric version of this reaction was preliminarily investigated.
The Iodine Atom Transfer Addition Reaction (I-ATRA) initiated by AIBN: Optimization, scope and radical reaction pathways
Balczewski, Piotr,Szadowiak, Aldona,Bialas, Tomasz
, p. 22 - 35 (2007/10/03)
Optimization of reaction conditions (alkene, halide, solvent, stoichiometry, manners of the reagents addition, and reaction time) of the I-ATRA reactions involving 1-iodoalkylphosphonates was carried out. GC-MS-CI/EI analyses showed main and side products of this reaction and the corresponding radical reaction pathways leading to products derived from phosphorus and nonphosphorus containing iodides, as well as explained the source of hydrogen in radical reduction processes accompanying the I-ATRA reaction. Synthesis of some 3-iodoalkyl and 3-iodoalkenylphosphonates was also presented based on the optimized procedure.
