6830-84-8 Usage
Description
Cyclohexanecarboxamide, N-methyl-, also known as N-methylcyclohexanecarboxamide, is a chemical compound with the molecular formula C8H15NO. It is an amide derivative featuring a cyclohexane ring and a methyl group attached to the nitrogen atom. Cyclohexanecarboxamide, N-methylis characterized by its low toxicity and is considered relatively safe for use in various industrial applications.
Uses
Used in Pharmaceutical Industry:
Cyclohexanecarboxamide, N-methylis used as a solvent in the pharmaceutical industry for the synthesis of various drugs and active pharmaceutical ingredients. Its ability to dissolve a wide range of compounds makes it a versatile solvent in drug manufacturing processes.
Used in Agrochemical Industry:
In the agrochemical industry, Cyclohexanecarboxamide, N-methylserves as a solvent for the production of pesticides, herbicides, and other crop protection agents. Its solubility properties allow for the efficient formulation of these chemicals, ensuring effective delivery to target pests and weeds.
Used in Plastics Industry:
Cyclohexanecarboxamide, N-methylis utilized as a solvent in the plastics industry for the manufacturing of various types of polymers and resins. Its compatibility with a range of monomers and polymers contributes to the production of high-quality plastic materials with desired properties.
Used as an Intermediate in Chemical Production:
Cyclohexanecarboxamide, N-methylis also used as an intermediate in the synthesis of other chemicals, including specialty amines, amides, and other organic compounds. Its reactivity and functional groups make it a valuable building block in organic chemistry.
Overall, Cyclohexanecarboxamide, N-methylis a versatile chemical compound with applications across multiple industries, primarily due to its solubility properties and low toxicity. Its use as a solvent and intermediate in various chemical processes highlights its importance in modern industrial chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6830-84-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6830-84:
(6*6)+(5*8)+(4*3)+(3*0)+(2*8)+(1*4)=108
108 % 10 = 8
So 6830-84-8 is a valid CAS Registry Number.
6830-84-8Relevant articles and documents
Dealkoxylation ofN-alkoxyamides without an external reductant driven by Pd/Al cooperative catalysis
Suzuki, Hirotsugu,Shiomi, Takahiro,Yoneoka, Kenji,Matsuda, Takanori
supporting information, p. 7545 - 7548 (2020/10/15)
Lewis acid-assisted palladium-catalysed dealkoxylation ofN-alkoxyamides has been developed. This reaction proceeded smoothly with a range ofN-alkoxyamides in the absence of an external reductant, thereby establishing a convenient and reductant-free protocol. In addition, a gram-scale reaction could be achieved. Preliminary mechanistic investigations indicated that β-hydrogen elimination from a palladium alkoxide intermediate generated an intramolecular hydride source.
Efficient one-stage procedure of Beckmann ketones rearrangement in the presence of hydroxylamine
Kuksenok,Shtrykova,Filimonov,Sidel'nikova
, p. 196 - 199 (2016/04/19)
Ketoximes formed from ketones in the presence of hydroxylamine and silica gel in formic acid undergo in situ the Beckmann rearrangement under mild conditions affording in high yields the corresponding amides. Unsymmetrical aromatic ketones, methyl aryl ketones, and methyl cyclohexyl ketone under these conditions form as a rule amides mixtures.
Highly Selective Hydrogenation of Aromatic Ketones and Phenols Enabled by Cyclic (Amino)(alkyl)carbene Rhodium Complexes
Wei, Yu,Rao, Bin,Cong, Xuefeng,Zeng, Xiaoming
supporting information, p. 9250 - 9253 (2015/08/11)
Air-stable Rh complexes ligated by strongly σ-donating cyclic (amino)(alkyl)carbenes (CAACs) show unique catalytic activity for the selective hydrogenation of aromatic ketones and phenols by reducing the aryl groups. The use of CAAC ligands is essential for achieving high selectivity and conversion. This method is characterized by its good compatibility with unsaturated ketones, esters, carboxylic acids, amides, and amino acids and is scalable without detriment to its efficiency.
