Welcome to LookChem.com Sign In|Join Free
  • or
1,3-Diphenyl-5-carbethoxy-1,2,4-triazole is a chemical compound with the molecular formula C18H15N3O2. It is a derivative of the 1,2,4-triazole ring system, featuring two phenyl groups attached to the 1 and 3 positions and a carbethoxy group at the 5 position. 1,3-diphenyl-5-carbethoxy-1,2,4-triazole is known for its potential applications in various fields, such as pharmaceuticals and agrochemicals, due to its unique structure and properties. It can be synthesized through various methods, including the reaction of phenylhydrazine with diazotized acetanilide, followed by cyclization. The compound is typically used as an intermediate in the synthesis of other more complex molecules, and its stability and reactivity make it a valuable component in the development of new drugs and chemical products.

1040-14-8

Post Buying Request

1040-14-8 Suppliers

Recommended suppliers

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

1040-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1040-14-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1040-14:
(6*1)+(5*0)+(4*4)+(3*0)+(2*1)+(1*4)=28
28 % 10 = 8
So 1040-14-8 is a valid CAS Registry Number.

1040-14-8Downstream Products

1040-14-8Relevant academic research and scientific papers

Tetrazole derivatives. 25. Investigation of the synthesis of 1-(5-tetrazolyl)-3,5-diphenylleucoverdazyl. Structure and some properties of the accompanying product - 1,3,7,9-tetraphenyl-5-oxo-5H-1,2,4-triazolo[3′,4′:5,1]imidazo[4,3-c] -1,2,4-triazole

Shchipanov,Klyuev

, p. 516 - 522 (1981)

In the reaction of 1,3-diphenyl-5-(5-tetrazolyl)formazan with formaldehyde, in addition to a leucoverdazyl, one can obtain 1,3-diphenyl-1,2,4-triazole and 1,3,7,9-tetraphenyl-5-oxo-5H-1,2,4-triazolo[3′,4′:5,1]imidazo[4,3-c]-1,2,4-triazole. The structure of the latter was established from data from the mass spectrum and the 1H and 13C NMR, UV, and IR spectra, as well as from the products of alcoholysis of this compound, which leads to 1,3-diphenyl-1,2,4-triazole and 1,3-diphenyl-5-carbethoxy-1,2,4-triazole. According to the data from the PMR spectra, the leucoverdazyl displays prototropic tautomerism due to the NH proton of the tetrazine ring.

REACTION OF 2,4,6-TRIPHENYLVERDAZYL WITH TRIFLUOROMETHYLSULFONYLCARBETHOXYDIBROMOMETHANE

Tomilenko, E. I.,Ogoiko, P. I.,Staninets, V. I.

, p. 1226 - 1228 (2007/10/02)

An unusual acylation of 2,4,6-triphenylverdazyl by trifluoromethylsulfonylcarbethoxydibromomethane in benzene has been discovered leading to 1-ethoxalyl-2,4,6-triphenyl-1,2,3,4-tetrahydro-sym-tetrazine (1-ethoxalyl-2,4,6-triphenylleukoverdazyl).

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 1040-14-8