17839-28-0 Usage
Description
(2,2-dimethylpropyl)ethylamine(SALTDATA: HCl), also known as HCl, is a chemical compound that consists of a tertiary amine and a hydrochloride salt. It is characterized by a lone pair of electrons and enhanced solubility in water due to its hydrochloride salt form. This versatile chemical serves as an important intermediate in the synthesis of various organic compounds and is commonly utilized as a reagent in organic synthesis and a catalyst in the preparation of pharmaceuticals and agrochemicals.
Uses
Used in Organic Synthesis:
(2,2-dimethylpropyl)ethylamine(SALTDATA: HCl) is used as a reagent in organic synthesis for its ability to act as an important intermediate in the synthesis of various organic compounds. Its unique structure and properties make it a valuable component in creating a wide range of chemical products.
Used in Pharmaceutical and Agrochemical Preparation:
In the pharmaceutical and agrochemical industries, (2,2-dimethylpropyl)ethylamine(SALTDATA: HCl) is used as a catalyst to facilitate the preparation of various products. Its role in these processes is crucial for enhancing the efficiency and effectiveness of the synthesis of drugs and agrochemicals.
Used in Chemical Research:
(2,2-dimethylpropyl)ethylamine(SALTDATA: HCl) is also utilized in chemical research as a versatile chemical with unique properties. Its application in research helps scientists explore new methods and develop innovative approaches in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 17839-28-0 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 17839-28:
(7*1)+(6*7)+(5*8)+(4*3)+(3*9)+(2*2)+(1*8)=140
140 % 10 = 0
So 17839-28-0 is a valid CAS Registry Number.
17839-28-0Relevant articles and documents
Highly unusual conversion of 1-alkyl-2-(bromomethyl)aziridines into 1-alkyl-2-(N-alkyl-N-ethylaminomethyl)aziridines using methyllithium
D'Hooghe, Matthias,Kimpe, Norbert De
, p. 1275 - 1277 (2008/02/02)
1-Alkyl-2-(bromomethyl)aziridines were transformed into 1-alkyl-2-(N-alkyl-N-ethylaminomethyl)aziridines upon treatment with 2-3 equiv. of methyllithium in THF or Et2O; the peculiarity in this transformation comprises the presence of an N-ethyl
N-heterocyclic inhibitors of TNF-alpha expression
-
, (2008/06/13)
N-heterocyclic compounds that block cytokine production via inhibition of p38 kinase are disclosed. In one embodiment, compounds of the present invention are represented by Formula I: Methods of production, pharmaceutical compositions and methods of treating conditions associated with inappropriate p38 kinase activity or TNF-α expression utilizing compounds of the present invention are also disclosed.
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.
