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1-[1-(4-methylphenyl)-1H-pyrrolo[2,3-b]quinoxalin-2-yl]cyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1408230-60-3

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1408230-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1408230-60-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,2,3 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1408230-60:
(9*1)+(8*4)+(7*0)+(6*8)+(5*2)+(4*3)+(3*0)+(2*6)+(1*0)=123
123 % 10 = 3
So 1408230-60-3 is a valid CAS Registry Number.

1408230-60-3Downstream Products

1408230-60-3Relevant academic research and scientific papers

Using Calcium Carbide as an Acetylene Source for Cascade Synthesis of Pyrrolo[2,3-b]quinoxalines via Copper-Free Sonogashira Coupling Reaction

Fakharian, Mahsa,Keivanloo, Ali,Nabid, Mohammad Reza

, (2018)

A palladium-catalyzed cascade protocol has been established for the synthesis of 4-methyl-1-(1H-pyrrolo[2,3-b]-quinoxalin-2-yl)cyclohexanols and 2-phenyl-1-(1H-pyrrolo[2,3-b]quinoxalin-2-yl)propan-1-ols through the reaction of N-alkyl(aryl)-3-chloroquinox

AlCl3 induced C-N bond formation followed by Pd/C-Cu mediated coupling-cyclization strategy: Synthesis of pyrrolo[2,3-b]quinoxalines as anticancer agents

Prasad, Bagineni,Shiva Kumar,Vijaya Babu,Anusha,Rambabu,Kandale, Ajit,Vanaja,Kalle, Arunasree M.,Pal, Manojit

, p. 6059 - 6066 (2012/11/07)

AlCl3 facilitated C-N bond forming reaction between 2,3-dichloroquinoxaline and anilines affording a convenient method for the preparation of N-aryl substituted 3-chloroquinoxalin-2-amines. A related N-benzyl derivative, however, was prepared via a conventional method. These N-alkyl/aryl substituted 3-chloroquinoxalin-2-amines on coupling with terminal alkynes in toluene under Pd/C-Cu catalysis afforded a range of 1,2-disubstituted pyrrolo[2,3-b]quinoxalines within 3-5 h in good to excellent yields. Some of the compounds synthesized showed promising anti-proliferative properties when tested in vitro against two cancer cell lines. Docking studies indicated that these molecules interact well with human Akt in silico.

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