Welcome to LookChem.com Sign In|Join Free
  • or
N-(2,5-dimethoxyphenyl)-4-methylquinolin-2-amine is a complex organic compound with the molecular formula C18H20N2O2. It is characterized by a quinoline-2-amine core, which features a quinoline ring system with an amine group attached to the 2-position. The quinoline ring is substituted with a 4-methyl group and a 2,5-dimethoxyphenyl group, which consists of a phenyl ring bearing two methoxy groups at the 2 and 5 positions. N-(2,5-dimethoxyphenyl)-4-methylquinolin-2-amine is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its structure and properties make it a subject of interest for researchers exploring new therapeutic agents and chemical intermediates.

5557-41-5

Post Buying Request

5557-41-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5557-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5557-41-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5557-41:
(6*5)+(5*5)+(4*5)+(3*7)+(2*4)+(1*1)=105
105 % 10 = 5
So 5557-41-5 is a valid CAS Registry Number.

5557-41-5Downstream Products

5557-41-5Relevant academic research and scientific papers

Divergent Asymmetric Total Synthesis of (+)-Vincadifformine, (-)-Quebrachamine, (+)-Aspidospermidine, (-)-Aspidospermine, (-)-Pyrifolidine, and Related Natural Products

Wang, Nengzhong,Du, Shuo,Li, Dong,Jiang, Xuefeng

, p. 3167 - 3170 (2017/06/23)

A uniformly strategic total synthesis of Aspidosperma alkaloids (+)-vincadifformine, (-)-quebrachamine, (+)-aspidospermidine, (-)-aspidospermine, (-)-pyrifolidine, and nine others from efficiently constructed tricyclic ketone 13 is reported. Highlights of these divergent and practical syntheses include (i) stereoselective intermolecular [4 + 2] cycloaddition to establish a C-E ring with one all-carbon quaternary stereocenter (C-5) and two bridged contiguous cis-stereocenters (C-12 and C-19), (ii) a Pd/C-catalyzed hydrogenation/deprotection/amidation cascade process to assemble the D ring, and (iii) Fischer indolization to forge the A-B ring.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5557-41-5