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17839-28-0

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17839-28-0 Usage

General Description

(2,2-dimethylpropyl)ethylamine, also known as HCl, is a chemical compound consisting of a tertiary amine and a hydrochloride salt. It is commonly used as a reagent in organic synthesis, and a catalyst in the preparation of pharmaceuticals and agrochemicals. As a tertiary amine, it possesses a lone pair of electrons, making it an important intermediate in the synthesis of various organic compounds. The hydrochloride salt form of the compound enhances its solubility in water, making it more easily handled and utilized in various chemical processes. Overall, (2,2-dimethylpropyl)ethylamine (HCl) is a versatile chemical with applications in organic synthesis and chemical research.

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.

17839-28-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-2,2-dimethylpropan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names N-Ethyl-2,2-dimethylpropylamin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17839-28-0 SDS

17839-28-0Downstream Products

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.

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