Welcome to LookChem.com Sign In|Join Free
  • or
1-methyl-3-phenyl-5,6,7,8-tetrahydroisoquinoline is a complex organic compound belonging to the isoquinoline family. It is characterized by a fused ring structure, with a methyl group attached to the 1-position and a phenyl group at the 3-position. The compound is a tetrahydro derivative, meaning that it contains four hydrogen atoms added across the isoquinoline ring, which reduces the number of double bonds and increases the saturation of the molecule. This particular chemical is known for its potential applications in medicinal chemistry, particularly in the synthesis of certain alkaloids and as a precursor in the production of pharmaceuticals. Its structure provides a foundation for further functionalization and exploration of its chemical properties and potential therapeutic uses.

1022-43-1

Post Buying Request

1022-43-1 Suppliers

Recommended suppliers

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

1022-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1022-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1022-43:
(6*1)+(5*0)+(4*2)+(3*2)+(2*4)+(1*3)=31
31 % 10 = 1
So 1022-43-1 is a valid CAS Registry Number.

1022-43-1Downstream Products

1022-43-1Relevant academic research and scientific papers

Pd(II)-Catalyzed Synthesis of Alicyclic[b]-Fused Pyridines via C(sp2)–H Activation of α,β-Unsaturated N-Acetyl Hydrazones with Vinyl Azides

Nie, Biao,Wu, Wanqing,Jin, Chuanfei,Ren, Qingyun,Zhang, Ji,Zhang, Yingjun,Jiang, Huanfeng

, p. 159 - 171 (2022/01/03)

A new synthetic protocol for alicyclic[b]-fused pyridines with complete regioselectivity from α,β-unsaturated N-acetyl hydrazones and vinyl azides via Pd(II)-catalyzed C–H activation/cyclization/aromatization strategy has been described. A series of five-

Access to Cycloalkeno[ c]-Fused Pyridines via Pd-Catalyzed C(sp2)-H Activation and Cyclization of N-Acetyl Hydrazones of Acylcycloalkenes with Vinyl Azides

Nie, Biao,Wu, Wanqing,Ren, Qingyun,Wang, Zhongqing,Zhang, Ji,Zhang, Yingjun,Jiang, Huanfeng

, p. 7786 - 7790 (2020/11/02)

A novel Pd(II)-catalyzed vinylic C-H activation and cyclization has been developed, reacting a series of small, medium, and large N-acetyl hydrazones of acylcycloalkenes with vinyl azides to access diverse cycloalkeno[c]-fused pyridine scaffolds. This protocol provides progress in C(sp2)-H bond activation of medium to large cycloalkenes, and the target products can be obtained in a specific regioselectivity with good functional group tolerance and a broad substrate scope.

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 1022-43-1