196703-47-6 Usage
Description
(R)-N-(Cyclohex-3-en-1-yl)acetaMide is a chemical compound characterized by the molecular formula C10H15NO. It is an acetamide derivative featuring a cyclohex-3-en-1-yl group attached to the nitrogen atom. (R)-N-(Cyclohex-3-en-1-yl)acetaMide is known for its unique structure and versatile reactivity, making it a valuable building block in both chemical and pharmaceutical research.
Uses
Used in Organic Synthesis:
(R)-N-(Cyclohex-3-en-1-yl)acetaMide is used as a reagent in organic synthesis for various chemical transformations. Its cyclohex-3-en-1-yl group provides a platform for further functionalization and modification, enabling the synthesis of a wide range of organic compounds.
Used in Coordination Chemistry:
In coordination chemistry, (R)-N-(Cyclohex-3-en-1-yl)acetaMide serves as a ligand, coordinating with metal ions to form stable complexes. Its ability to chelate metals enhances the stability and reactivity of the resulting complexes, making it a useful component in the design of metal-based catalysts and materials.
Used in Catalysis:
(R)-N-(Cyclohex-3-en-1-yl)acetaMide can also function as a catalyst or a catalyst precursor in various chemical reactions. Its presence can facilitate or accelerate specific transformations, improving the efficiency and selectivity of the processes.
Used in Pharmaceutical Research and Development:
(R)-N-(Cyclohex-3-en-1-yl)acetaMide holds potential in the pharmaceutical industry, particularly in the development of new drugs and medications. Its unique structure and reactivity make it a promising candidate for the design of novel therapeutic agents, targeting a variety of diseases and conditions.
Used in Drug Delivery Systems:
In the field of drug delivery, (R)-N-(Cyclohex-3-en-1-yl)acetaMide can be employed to improve the bioavailability and therapeutic efficacy of existing drugs. Its ability to form stable complexes with metal ions and other molecules allows for the development of innovative drug delivery systems, enhancing the performance of pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 196703-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,7,0 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 196703-47:
(8*1)+(7*9)+(6*6)+(5*7)+(4*0)+(3*3)+(2*4)+(1*7)=166
166 % 10 = 6
So 196703-47-6 is a valid CAS Registry Number.
196703-47-6Relevant articles and documents
Synthesis of new 7-azabicyclo[2.2.1]heptane derivatives
Marco-Contelles, Jose,Gomez-Sanchez, Elena,Samadi, Abdelouahid,Soriano, Elena,Valderas, Carolina,Alvarez-Perez, Monica,Do Carmo Carreiras, Mria
experimental part, p. 56 - 73 (2010/08/20)
The synthesis of new 7-azabicyclo[2.2.1]heptane derivatives has been achieved in a four-step synthetic sequence, starting from readily available cyclohex-3-enecarboxylic acid, Curtius reaction, stereoselective bromination leading to major benzyl(cis-3, tr
RITTER REACTION WITH CYCLOPROPYL KETONES AND CYCLOPROPYL ALCOHOLS: SYNTHESIS OF N-ACYL-γ-KETO AND N-ACYL HOMOALLYL AMINES
Vankar, Y. D.,Kumaravel, G.,Rao, C. T.
, p. 2181 - 2198 (2007/10/02)
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