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N-cyclopropyl-N-ethylamine is an organic compound with the molecular formula C5H11N. It is characterized by the presence of a cyclopropyl ring, which is a three-carbon atom ring, and an ethylamine group, a primary amine with a two-carbon chain replacing one hydrogen atom. N-cyclopropyl-N-ethylamine is widely used as an intermediate in various organic synthesis processes.

26389-72-0

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26389-72-0 Usage

Uses

Used in Chemical Synthesis:
N-cyclopropyl-N-ethylamine is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-cyclopropyl-N-ethylamine is used as a building block for the development of new drugs. Its ability to form stable bonds with other molecules makes it a key component in the synthesis of certain medications, contributing to their therapeutic effects.
Used in Agrochemical Industry:
N-cyclopropyl-N-ethylamine is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection products. Its reactivity and compatibility with other chemical compounds enable the creation of effective and targeted agrochemicals that protect crops from pests and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 26389-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,3,8 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26389-72:
(7*2)+(6*6)+(5*3)+(4*8)+(3*9)+(2*7)+(1*2)=140
140 % 10 = 0
So 26389-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H11N/c1-2-6-5-3-4-5/h5-6H,2-4H2,1H3

26389-72-0Downstream Products

26389-72-0Relevant academic research and scientific papers

PGD2 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISEASES

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Page/Page column 98-99, (2008/06/13)

Disclosed are CRTH2 inhibitors represented by Structural Formula (I). The values for the variables of Structural Formula (I) are provided herein.

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.

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