Welcome to LookChem.com Sign In|Join Free
  • or
Diethyl (4-methylphenyl)thiocarbamamoylmalonate is a complex organic chemical compound with the molecular formula C16H20N2O4S. It is a derivative of thiocarbamic acid, featuring a 4-methylphenyl group attached to the thiocarbamoylmalonate moiety. diethyl (4-methylphenyl)thiocarbamamoylmalonate is characterized by its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a precursor in the production of fungicides and herbicides. Its structure includes two ethyl ester groups, which can be hydrolyzed to form the corresponding acids, and a sulfur atom bonded to the nitrogen in the thiocarbamoyl group, contributing to its reactivity and chemical properties. The compound's specific role in chemical synthesis and its potential impact on the development of new chemicals make it an important molecule in the field of organic chemistry.

3288-13-9

Post Buying Request

3288-13-9 Suppliers

Recommended suppliers

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

3288-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3288-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3288-13:
(6*3)+(5*2)+(4*8)+(3*8)+(2*1)+(1*3)=89
89 % 10 = 9
So 3288-13-9 is a valid CAS Registry Number.

3288-13-9Relevant academic research and scientific papers

Rearrangements of 2-pyridyl-3-arylaminoisoxazol-5(2H)-ones to imidazo[1,2-a]pyridines under flash-vacuum-pyrolysis

Setamdideh, Davood,Khanahmadzadeh, Salah,Khorshidi, Nasrin

experimental part, p. 2884 - 2890 (2012/07/17)

2-Pyridyl-3-arylaminoisoxazol-5(2H)-ones, rearranged under flash-vacuum-pyrolysis (FVP) conditions accompanied by elimination of carbon dioxide to give imidazo[1,2-a]pyridines in high to excellent yields (85-95 %).

Synthesis of 2-(5-nitropyrid-2-yl)-3-(4-substitutedphenyl)aminoisoxazol- 5(2h)-ones and their rearrangements to imidazo[1,2-a]-pyridines and indoles with triethylamine

Khalafy,Setamdideh,Dilmaghani, K. Akbari

, p. 907 - 916 (2007/10/03)

3-(4-Substitutedphenyl)aminoisoxazol-5(2H)-ones, substituted on nitrogen with a nitropyridine group, react with triethylamine to give imidazo[1,2-a]pyridines and indoles. With 4-bromophenyl and 4-methylphenyl group substituents only imidazopyridines are f

2-Aryl-3-arylaminoisoxazol-5(2H)-ones as sources of indoles and imidazo[1,2-a]pyridines

Jeffery, David,Prager, Rolf H,Turner, David,Dreimanis, Monica

, p. 9965 - 9972 (2007/10/03)

2-Aryl-3-arylaminoisoxazol-5(2H)-ones undergo solvolysis to form 1,3-dipoles that undergo intramolecular cyclisation to form either imidazopyridines or indoles. The mode of cyclisation is controlled by the electronegativity of the aryl substituents.

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 3288-13-9