61995-24-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This is the widely recognized name for the compound, which is derived from its parent compound, caprolactam.
Explanation
The compound has a cyclic structure with an amide functional group, which is a carbonyl group (C=O) bonded to a nitrogen atom and two other substituents.
Explanation
The compound contains an amide group (-CONH-), an ester group (-COOCH3), and a methyl group (-CH3) as its main functional groups.
Explanation
Caprolactam methyl ester is used in the production of various chemical products, including those in the pharmaceutical, pesticide, and plastic industries.
Explanation
The compound is commonly utilized as an intermediate in organic synthesis due to its reactive functional groups and cyclic structure.
Explanation
The compound's cyclic structure and functional groups make it a potential building block for the synthesis of biologically active molecules in the pharmaceutical industry.
Explanation
Caprolactam methyl ester can also be used as a solvent or reagent in various chemical reactions due to its reactivity and functional groups.
Chemical Structure
Cyclic Amide
Functional Groups
Amide, Ester, and Methyl
Applications
Pharmaceutical, Pesticides, and Plastics
Intermediate in Organic Synthesis
Yes
Potential Applications
Synthesis of Biologically Active Molecules
Additional Uses
Solvent or Reagent in Chemical Reactions
Check Digit Verification of cas no
The CAS Registry Mumber 61995-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,9 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61995-24:
(7*6)+(6*1)+(5*9)+(4*9)+(3*5)+(2*2)+(1*4)=152
152 % 10 = 2
So 61995-24-2 is a valid CAS Registry Number.
61995-24-2Relevant academic research and scientific papers
Synthesis of α-hydroxyalkyl dehydroazepanes via catalytic enantioselective borylative migration of an enol nonaflate
Clement, Helen A.,Hall, Dennis G.
supporting information, p. 4334 - 4339 (2018/11/10)
A Pd-catalyzed borylative migration methodology for cyclic enol perfluorosulfonates was applied to the synthesis of the corresponding 7-membered, azepane ring system. Throughout the optimization, it was shown that the reaction is sensitive to the nitrogen protecting group as well as the type of base and solvent. The resulting cyclic allylboronate reacts stereoselectively with aldehydes for the synthesis of novel α-hydroxyalkyl dehydroazepanes in good yield and enantioselectivity over two steps. We highlight the utility of this methodology with an efficient synthesis of the de novo 7-membered ring analogue of the piperidine alkaloid β-conhydrine.
