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-(4-acetylphenyl)-1,2,4-triazolidine-3,5-dione (Cas 959864-55-2)

-(4-acetylphenyl)-1,2,4-triazolidine-3,5-dione (Cas 959864-55-2)

3500 INR/Kilograms

Product Details:

  • Solubility Chloroform (Sparingly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Sli
  • Taste Bitter
  • Storage Room Temperature
  • Melting Point >140°C (dec.)
  • Molecular Weight 175.14 GSM (gm/2)
  • Structural Formula C8H5N3O2;
  • Shelf Life 5 Years
  • Supply Ability : 10000 Kilograms Per Month
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Price And Quantity

  • 3500 INR/Kilograms
  • 3500.00 - 5000.00 INR/Kilograms
  • 100kg Kilograms

Product Specifications

  • 4-Phenyl-1,2,4-triazoline-3,5-dione
  • 337380
  • Industrial Grade
  • 4-Phenyl-1,2,4-triazoline-3,5-dione
  • 6
  • C8H5N3O2;
  • Popcorn
  • red solid
  • Chloroform (Sparingly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Sli
  • Bitter
  • Room Temperature
  • >140°C (dec.)
  • 99%
  • 4-Phenyl-1,2,4-triazoline-3,5-dione (PTAD) can be used: As a dehydrogenating agent to synthesize annulated dihydropyridazines by inverse [4+2] cycloaddition reaction between cyclic alkenes, and 1,2,4,5-tetrazines. As a dienophile to synthesize cycloaddition products by fast hetero-Diels−Alder reactions 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione; 4-Phenyl-Δ1-1,2,4-triazoline-3,5-dione; 4-Phenyl-3,5-Dioxotriazole; 4-Phenyldehydrourazole; Azodicarboxylic Acid N-Phenylimide; N-Phenylazodicarboximide; N-Phenylazodicarboxylic Imide; N-Phenyltriazolinedione
  • 175.14 GSM (gm/2)
  • 4233-33-4
  • C8H5N3O2;
  • Powder
  • 5 Years
  • Pharmaceutical Intermediates
  • 4343-76-9

Trade Information

  • GOA
  • 10000 Kilograms Per Month
  • 21 Days
  • Within a certain price range free samples are available
  • 50*1
  • Africa, Middle East, Western Europe, Eastern Europe, South America, North America, Central America, Australia, Asia
  • All India

Product Description

4-Phenyl-1,2,4-triazoline-3,5-dione (PTAD) is an azodicarbonyl compound. PTAD is one of the strongest dienophiles and reacts rapidly with dienes in Diels-Alder reactions.[1] The most prominent use of PTAD was the first successful synthesis of prismane in 1973.


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