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(3-Chloro-quinoxalin-2-yl)-Methyl-aMine is a chemical compound characterized by a quinoxaline ring with a 3-chloro substitution and a methylamine group attached to the second position of the quinoxaline ring. It is known for its reactive nature and structural versatility, making it a valuable intermediate in the synthesis of pharmaceutical compounds and agrochemicals. Its potential biological activities and pharmacological properties also contribute to its significance in medicinal chemistry.

90537-58-9

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90537-58-9 Usage

Uses

Used in Pharmaceutical Synthesis:
(3-Chloro-quinoxalin-2-yl)-Methyl-aMine is used as an intermediate in the synthesis of various pharmaceutical compounds. Its structural versatility allows for the creation of a wide range of drugs and bioactive compounds, making it a crucial component in the development of new medications.
Used in Agrochemical Production:
In the agrochemical industry, (3-Chloro-quinoxalin-2-yl)-Methyl-aMine is utilized as an intermediate for the synthesis of various agrochemicals. Its reactive nature enables the production of compounds with specific properties tailored to agricultural applications, such as pest control and crop protection.
Used in Medicinal Chemistry Research:
(3-Chloro-quinoxalin-2-yl)-Methyl-aMine is also used in the field of medicinal chemistry for studying its potential biological activities and pharmacological properties. This research can lead to the discovery of new therapeutic agents and contribute to the advancement of medical treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 90537-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,3 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90537-58:
(7*9)+(6*0)+(5*5)+(4*3)+(3*7)+(2*5)+(1*8)=139
139 % 10 = 9
So 90537-58-9 is a valid CAS Registry Number.

90537-58-9Relevant academic research and scientific papers

Synthesis of unexpected pyrrolo[2,3- b ]quinoxaline-2-carbaldehydes via sonogashira coupling reaction

Keivanloo, Ali,Bakherad, Mohammad,Rahimi, Amin

experimental part, p. 1599 - 1602 (2010/06/19)

The reaction of a number of N-alkyl-3-chloroquinoxaline-2-amines with propargyl bromide in the presence of PdClPPhand copper(I) iodide in wet morpholine leads to the formation of the unexpected N-substituted pyrrolo[2,3-b]quinoxaline-2-carbaldehydes in good yields. A possible mechanism for the conversion is suggested. Georg Thieme Verlag Stuttgart.

One-pot synthesis of 1,2-disubstituted pyrrolo[2,3-b]quinoxalines via palladium-catalyzed heteroannulation in water

Keivanloo, Ali,Bakherad, Mohammad,Rahimi, Amin,Taheri, Sayed Ali Naghi

experimental part, p. 2409 - 2412 (2010/06/21)

The reaction of N-alkyl-3-chloroquinoxaline-2-amines with 1-alkynes, catalyzed by Pd-Cu, in the presence of sodium lauryl sulfate as the surfactant in water, leads to the one-pot formation of 1,2-disubstituted pyrrolo[2,3-b]quinoxalines in good-to-high yields.

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