Welcome to LookChem.com Sign In|Join Free
  • or
2-Propanone, 1-(3,5-diphenyl-1,3,4-thiadiazol-2(3H)-ylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80746-24-3

Post Buying Request

80746-24-3 Suppliers

Recommended suppliers

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

80746-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80746-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,4 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80746-24:
(7*8)+(6*0)+(5*7)+(4*4)+(3*6)+(2*2)+(1*4)=133
133 % 10 = 3
So 80746-24-3 is a valid CAS Registry Number.

80746-24-3Downstream Products

80746-24-3Relevant academic research and scientific papers

2-Alkyl-3,5-diaryl-1,3,4-thiadiazolium Perchlorates and Reactions thereof

Mastalerz, Harold,Gibson, Martin S.

, p. 245 - 249 (2007/10/02)

2-Alkyl- and 2-aryl-3,5-diaryl-1,3,4-thiadiazolium perchlorates can be prepared from N'-arylbenzothiohydrazides by reaction with (a) a carboxylic anhydride-perchloric acid mixture or (b) a nitrile-perchloric acid mixture.The 2-methyl-3,5-diaryl-1,3,4-thia

Routes to 3-Aryl-5-phenyl-2-thioacylmethylene-2H-1,3,4-thiadiazolenes

Mastalerz, Harold,Gibson, Martin S.

, p. 2952 - 2955 (2007/10/02)

Prospective routes to the above compounds include reaction of an N'-arylbenzothiohydrazide or of its N'-acetyl derivative with thioacetic acid, when the thioacyl and acyl derivatives are formed, as well as by reaction of the 2-acylmethylene-3-aryl-5-pheny

Acylation of N'-Arylbenzothiohydrazides and of their N'-Acyl-derivatives; 2-Acylalkylidene-3-aryl-5-phenyl-2H-1,3,4-thiadiazolenes and Related Compounds

Callaghan, Patrick D.,Elliott, Arthur J.,Gandhi, Sham S.,Gibson, Martin S.,Mastalerz, Harold,Vukov, Darko J.

, p. 2948 - 2951 (2007/10/02)

Reactions of N'-arylbenzothiohydrazides and of their N-acyl-derivatives with carboxylic anhydrides under various sets of conditions are shown to lead to 2-acylalkylidene-3-aryl-5-phenyl-2H-1,3,4-thiadiazolenes.The probable mechanism of formation of these compounds via the corresponding 2-alkylidenethiadiazolene as intermediate is discussed.

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 80746-24-3