4701-95-5 Usage
Uses
Used in Pharmaceutical Synthesis:
(1Z)-3-methylcyclohexanone oxime is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and improving existing ones.
Used in Pesticide Production:
(1Z)-3-methylcyclohexanone oxime is utilized as a precursor in the production of pesticides, helping to create effective and safer agrochemicals for agricultural applications.
Used in Rubber Chemicals:
(1Z)-3-methylcyclohexanone oxime is employed as a building block in the creation of rubber chemicals, enhancing the properties and performance of rubber products.
Used as a Reagent in Organic Chemistry:
(1Z)-3-methylcyclohexanone oxime is used as a reagent in various organic chemistry reactions, particularly in the preparation of heterocyclic compounds and as a protecting group for carbonyl compounds, facilitating complex organic synthesis.
Used in Adhesives, Sealants, and Coatings Manufacturing:
(1Z)-3-methylcyclohexanone oxime is used as a stabilizer or inhibitor in the manufacturing of adhesives, sealants, and coatings. It helps prevent degradation caused by exposure to oxygen, heat, or UV radiation, thereby improving the durability and performance of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 4701-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4701-95:
(6*4)+(5*7)+(4*0)+(3*1)+(2*9)+(1*5)=85
85 % 10 = 5
So 4701-95-5 is a valid CAS Registry Number.
4701-95-5Relevant academic research and scientific papers
Synthesis of amides with anti-inflammatory and analgesic activities
Pau,Cerri,Boatto,Palomba,Pintore,Filippelli,Falcone,Palagiano,Rossi
, p. 93 - 98 (2007/10/03)
A series of N-Aroyl-cyclohexyl- and cyclohexenylamides 3- or 4- methylsubstituted were synthesized and evaluated for their anti-inflammatory and analgesic potencies, and gastrointestinal irritation liability. One compound, N-benzoyl-4-methyl-cyclohexylamide 6a, possessed an anti- inflammatory activity comparable to that of indomethacin.
Asymmetric syntheses of 3-substituted-cyclohexanone derivatives by stereoselective conjugate addition to chiral 2-substituted-2-cyclohexen-1-ones
Schultz, Arthur G.,Harrington, Roger E.
, p. 4926 - 4931 (2007/10/02)
Chiral 2-substituted-2-cyclohexen-1-one 2a is prepared from 1a by Birch reduction followed by acid-catalyzed hydrolysis-olefin migration. Conjugate additions of organometallic reagents to 2a occur with good to excellent diastereoselectivities (Table I). E
