Welcome to LookChem.com Sign In|Join Free
  • or
1-methyl-2-tosyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole is a complex organic compound with the molecular formula C18H20N2O2S. It is a derivative of the pyridoindole class of compounds, which are known for their potential biological activities. This specific compound features a pyridoindole core, with a methyl group at the 1-position, a tosyl (tosylate) group at the 2-position, and a fully saturated ring system, indicating the presence of four hydrogen atoms on the carbon atoms that would otherwise form part of the aromatic structure. The compound's structure and properties make it a subject of interest in medicinal chemistry, particularly for its potential applications in the development of new drugs and therapeutic agents. Its synthesis and biological evaluation are areas of active research, as modifications to the pyridoindole scaffold can lead to compounds with diverse pharmacological profiles.

5159-20-6

Post Buying Request

5159-20-6 Suppliers

Recommended suppliers

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

5159-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5159-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5159-20:
(6*5)+(5*1)+(4*5)+(3*9)+(2*2)+(1*0)=86
86 % 10 = 6
So 5159-20-6 is a valid CAS Registry Number.

5159-20-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2-(toluene-4-sulfonyl)-2,3,4,9-tetrahydro-1H-β-carboline

1.2 Other means of identification

Product number -
Other names N-Tosyltetrahydroharman

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5159-20-6 SDS

5159-20-6Downstream Products

5159-20-6Relevant academic research and scientific papers

Dehydrogenation of N-Heterocycles by Superoxide Ion Generated through Single-Electron Transfer

Huang, Yuan-Qiong,Song, Hong-Jian,Liu, Yu-Xiu,Wang, Qing-Min

supporting information, p. 2065 - 2069 (2018/01/27)

Nitrogen-containing heteroarene motifs are found in numerous pharmaceuticals, natural products, and synthetic materials. Although several elegant methods for synthesis of these compounds through dehydrogenation of the corresponding saturated heterocycles have been reported, some of the methods are hampered by long reaction times, harsh conditions, and the need for catalysts that are not readily available. This work reports a novel method for dehydrogenation of N-heterocycles. Specifically, O2.? generated in situ acts as the oxidant for N-heterocycle substrates that are susceptible to oxidation through a hydrogen atom transfer mechanism. This method provides a general, green route to N-heteroarenes.

Efficient and practical one-pot conversions of n- tosyltetrahydroisoquinolines into isoquinolines and of N-tosyltetrahydro-β- carbolines into β-carbolines through tandem β-elimination and aromatization

Dong, Jing,Shi, Xiao-Xin,Yan, Jing-Jing,Xing, Jing,Zhang, Qiang,Xiao, Sen

experimental part, p. 6987 - 6992 (2011/02/24)

An efficient, practical, and general method for conversions of N-tosyltetrahydroisoquinolines (N-tosyl-THIQs) into isoquinolines and of N-tosyltetrahydro-β-carbolines (N-tosyl-THBCs) into β-carbolines is described. Treatment of N-tosyl-THIQs or N-tosyl-THBCs with base in dimethyl sulfoxide afforded dihydroisoquinolines or dihydro-β-carbolines as intermediates, and these were then oxidized in situ by molecular oxygen to furnish isoquinolines or β-carbolines in good to high yields. Both one-pot conversions occurred through tandem β-elimination and aromatization. An efficient method for conversions ofN-tosyltetrahydroisoquinolines (N-tosyl-THIQs) and N-tosyltetrahydro-β-carbolines (N-tosyl-THBCs) into isoquinolines and β-carbolines is described. Treatment ofN-tosyl-THIQs or N-tosyl-THBCs with base affords dihydroisoquinolines or dihydro-β- carbolines. These can be oxidized in situ by molecular oxygen to furnish isoquinolines or β-carbolines. Copyright

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 5159-20-6