47304-99-4 Usage
Uses
Used in Chemical Synthesis:
Bis(2-naphthalenylMethyl)aMine is used as a key intermediate in the synthesis of primary amines through a nitrogen-doped carbon-supported cobalt-nanocatalyzed reductive amination of aldehydes. This process is significant in the production of various chemical compounds and materials, as primary amines are essential building blocks in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Bis(2-naphthalenylMethyl)aMine is utilized as a precursor for the development of novel drug candidates. Its unique structure and reactivity make it a promising starting material for the synthesis of new therapeutic agents, potentially targeting a wide range of medical conditions.
Used in Material Science:
Bis(2-naphthalenylMethyl)aMine is also employed in the field of material science, particularly in the development of advanced materials with specific properties. Its incorporation into polymers and other materials can lead to improved performance characteristics, such as enhanced stability, increased strength, or tailored optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 47304-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,3,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 47304-99:
(7*4)+(6*7)+(5*3)+(4*0)+(3*4)+(2*9)+(1*9)=124
124 % 10 = 4
So 47304-99-4 is a valid CAS Registry Number.
47304-99-4Relevant academic research and scientific papers
N-Alkylation of Aqueous Ammonia with Alcohols Leading to Primary Amines Catalyzed by Water-Soluble N-Heterocyclic Carbene Complexes of Iridium
Fujita, Ken-Ichi,Furukawa, Shohichi,Morishima, Namino,Shimizu, Mineyuki,Yamaguchi, Ryohei
, p. 1993 - 1997 (2018/03/13)
A new catalytic system for the N-monoalkylation of aqueous ammonia with a variety of alcohols was developed. Water-soluble dicationic complexes of iridium bearing N-heterocyclic carbene and diammine ligands exhibited high catalytic activity for this type of reaction on the basis of hydrogen-transfer processes without generating harmful or wasteful byproducts. Various primary amines were efficiently synthesized by using safe, inexpensive, and easily handled aqueous ammonia as a nitrogen source. For example, the reaction of 1-(4-methylphenyl)ethanol with aqueous ammonia in the presence of a water-soluble N-heterocyclic carbene complex of iridium at 150 °C for 40 h gave 1-(4-methylphenyl)ethylamine in 83 % yield.
A biomimetic electrocatalytic system for the atom-economical chemoselective synthesis of secondary amines
Largeron, Martine,Fleury
supporting information; experimental part, p. 883 - 886 (2009/07/25)
A facile one-pot oxidation-imine formation-reduction route to secondary amines can be achieved electrolytically from primary amines. This atom-economical 1ox-mediated sequence, leaving ammonia as the sole byproduct, allows the rapid chemoselect
