Welcome to LookChem.com Sign In|Join Free
  • or
3-benzoyl-2H-chromene-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1142124-79-5

Post Buying Request

1142124-79-5 Suppliers

Recommended suppliers

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

1142124-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1142124-79-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,2,1,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1142124-79:
(9*1)+(8*1)+(7*4)+(6*2)+(5*1)+(4*2)+(3*4)+(2*7)+(1*9)=105
105 % 10 = 5
So 1142124-79-5 is a valid CAS Registry Number.

1142124-79-5Downstream Products

1142124-79-5Relevant academic research and scientific papers

Synthesis of chromene-2-thiones and in vitro evaluation of their antifungal and antibacterial activities

Devi, Nepram Sushuma,Singh, Thokchom Prasanta,Khumanthem, Nonibala,Singh, Okram Mukherjee

, p. 1224 - 1231 (2013/10/08)

Cyclocondensation of β-oxodithioesters with substituted 2- hydroxy benzaldehydes in presence of copper(II)chloride as the catalyst yields 3-alkanoyl/aroyl/heteroaroyl-2H-chromene-2- thiones (87-95% yields). These reactions are carried out under solvent-fr

An expedient route to highly functionalized 2H-chromene-2-thiones via ring annulation of β-oxodithioesters catalyzed by InCl3 under solvent-free conditions

Verma, Rajiv Kumar,Verma, Girijesh K.,Raghuvanshi, Keshav,Singh, Maya Shankar

, p. 584 - 589 (2011/03/18)

A convenient and one-pot synthesis of 3-aroyl/heteroaroyl-2H-chromene-2- thiones and benzo[f]2H-chromene-2-thiones has been developed by the condensation of β-oxodithioesters and salicylaldehydes/α-hydroxynaphthaldehydes in the presence of indium trichlor

Novel 3-alkanoyl/aroyl/heteroaroyl-2H-chromene-2-thiones: Synthesis and evaluation of their antioxidant activities

Singh, Okram Mukherjee,Devi, Nepram Sushuma,Thokchom, Dhanaraj Singh,Sharma, Gurumayum Jitendra

experimental part, p. 2250 - 2257 (2010/06/15)

A facile, convenient and high yielding synthesis of a combinatorial library of 3-alkanoyl/aroyl/heteroaroyl-2H-chromene-2-thiones has been developed by the condensation of easily accessible β-oxodithioesters and salicylaldehyde/substituted 2-hydroxybenzal

Biginelli and Hantzsch-type reactions leading to highly functionalized dihydropyrimidinone, thiocoumarin, and pyridopyrimidinone frameworks via ring annulation with β-oxodithioesters

Nandi, Ganesh Chandra,Samai, Subhasis,Singh, Maya Shankar

supporting information; experimental part, p. 7785 - 7795 (2011/02/21)

An efficient and highly convergent route to dihydropyrimidinones (DHPMs) and hitherto unreported dihydropyridopyrimidinones has been developed by one-pot, three-component cyclocondensation of aromatic aldehydes, β-oxodithioesters, and urea/6-amino-1,3-dim

Application of β-Oxodithioesters in domino and multicomponent reactions: Facile route to dihydropyrimidines and coumarins

Singh, Okram Mukherjee,Devi, Nepram Sushuma

supporting information; experimental part, p. 3141 - 3144 (2009/08/15)

A facile route to hitherto unknown 5-methylmercaptothiocarbonyl-4-aryl-3,4- dihydropyrimidin-2(1H)-ones and substituted 2H-chromene-2-thiones has been developed. SnCl2catalyzed cyclocondensation of β-oxodithioesters with a variety of readily ac

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 1142124-79-5