17839-26-8 Usage
Uses
Used in Pharmaceutical Synthesis:
N-Ethyl-Pentylamine is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows it to be a valuable building block in the creation of new and effective medications.
Used in Polymer and Plastic Production:
In the chemical industry, N-Ethyl-Pentylamine serves as a crucial component in the production of polymers and plastics. Its ability to react with other compounds makes it an essential ingredient in the formulation of various types of plastics with specific properties.
Used as a Fuel Additive:
N-Ethyl-Pentylamine is utilized as a fuel additive to improve the performance and efficiency of fuels. Its addition can enhance combustion, reduce emissions, and provide other benefits to the fuel's overall performance.
Used in Corrosion Inhibitor Manufacturing:
In the manufacturing of corrosion inhibitors, N-Ethyl-Pentylamine plays a significant role. Its chemical properties make it suitable for creating compounds that can protect metals from corrosion, extending their lifespan and improving their durability.
Overall, N-Ethyl-Pentylamine is a versatile chemical compound with a wide range of applications across different industries, from pharmaceuticals to fuel additives, demonstrating its importance in modern chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 17839-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,3 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17839-26:
(7*1)+(6*7)+(5*8)+(4*3)+(3*9)+(2*2)+(1*6)=138
138 % 10 = 8
So 17839-26-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H17N/c1-3-5-6-7-8-4-2/h8H,3-7H2,1-2H3
17839-26-8Relevant academic research and scientific papers
Preparation process of aminoacetamide derivative
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, (2008/06/13)
Disclosed herein are novel processes for preparing aminoacetamide derivatives, wherein: (1) a secondary amine is reacted with a 2-haloacetamide in the presence or absence of at least one solvent selected from water, lower alcohols, aromatic solvents and acetic acid esters; (2) an N-benzylideneamine derivative is reacted with dimethyl sulfate or diethyl sulfate to form a secondary amine, and this secondary amine is then reacted with a 2-haloacetamide; and (3) a primary amine is reacted with benzaldehyde to form an N-benzylideneamine derivative, this product is then reacted with dimethyl sulfate or diethyl sulfate to form a secondary amine, and this secondary amine is further reacted with a 2-haloacetamide. The 2-aminoacetamide derivatives are useful as intermediates for the preparation of novel antibiotics.
ELECTROCHEMICAL REDUCTIVE AMINATION. II. AMINATION OF ALIPHATIC ALDEHYDES WITH PRIMARY AMINES
Smirnov, Yu. D.,Pavlichenko, V. F.,Tomilov, A. P.
, p. 374 - 380 (2007/10/02)
The formation of a secondary amine by the electrolysis of an aqueous solution containing an aldehyde and a primary amine was studied.The formation of the secondary amines passes through the intermediate stage of an aldimine.The highest yield of secondary amine is attained at a molar ratio of primary amine to aldehyde of 1.2:1.As electrode material lead, cadmium, zinc, and copper may be used.As supporting electrolyte a phosphate buffer with a pH close to the pKa of the primary amine is recommended.By the method developed 32 amines with various structures were synthesized.
