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4-Ethoxy-6-methoxy-2-phenyl-1,2,3,4-tetrahydro-quinoline is a complex organic compound belonging to the quinoline family. It is characterized by a quinoline ring structure, which is fused to a tetrahydro ring, and features a phenyl group at the 2-position. The molecule also contains an ethoxy group at the 4-position and a methoxy group at the 6-position, which contribute to its overall structure and properties. 4-ethoxy-6-methoxy-2-phenyl-1,2,3,4-tetrahydro-quinoline is known for its potential applications in the pharmaceutical and chemical industries, particularly as a precursor in the synthesis of various drugs and other organic compounds. Its unique structure and functional groups make it an interesting target for further research and development in the field of organic chemistry.

5568-58-1

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5568-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5568-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5568-58:
(6*5)+(5*5)+(4*6)+(3*8)+(2*5)+(1*8)=121
121 % 10 = 1
So 5568-58-1 is a valid CAS Registry Number.

5568-58-1Downstream Products

5568-58-1Relevant academic research and scientific papers

Ln(OTf)3- or Sc(OTf)3-Catalyzed Three Components Coupling Reactions between Aldehydes, Amines, and Dienes or Alkenes. Efficient Syntheses of Pyridine and Quinoline Derivatives

Kobayashi, Shu,Ishitani, Haruro,Nagayama, Satoshi

, p. 423 - 424 (1995)

Three components coupling reactions between aldehydes, amines, and dienes or alkenes were catalyzed by lanthanide or scandium triflate to afford pyridine and quinoline derivatives in high yields.The Lewis acid catalysts were stable and kept their activity

Bismuth(III) chloride and triflate: New efficient catalysts for the Aza-Diels-Alder reaction

Laurent-Robert,Garrigues,Dubac

, p. 1160 - 1162 (2007/10/03)

Bismuth(III) chloride (1) and triflate (2) are excellent catalysts of hetero Diels-Alder reactions of imines 3-6 with diene 7 or dienophiles 8 and 9. A one-pot procedure with in situ production of imine from the corresponding aldehyde and amine was possib

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