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1,3-DIETHYL-5,6-DIAMINOURACIL

  • CAS No.:52998-22-8
  • Purity:99%
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1,3-DIETHYL-5,6-DIAMINOURACIL Good Manufacturer supply High Quality 52998-22-8

  • Molecular Formula:C8H14N4O2
  • Molecular Weight:198.225
  • Vapor Pressure:0.0043mmHg at 25°C 
  • Melting Point:88-98°C 
  • Refractive Index:1.548 
  • Boiling Point:278.3°Cat760mmHg 
  • PKA:4.40±0.70(Predicted) 
  • Flash Point:122.1°C 
  • PSA:96.04000 
  • Density:1.23g/cm3 
  • LogP:0.37660 

1,3-DIETHYL-5,6-DIAMINOURACIL(Cas 52998-22-8) Usage

InChI:InChI=1/C8H14N4O2/c1-3-11-6(10)5(9)7(13)12(4-2)8(11)14/h3-4,9-10H2,1-2H3

52998-22-8 Relevant articles

Novel, Dual Target-Directed Annelated Xanthine Derivatives Acting on Adenosine Receptors and Monoamine Oxidase B

Brockmann, Andreas,Doroz-P?onka, Agata,Ja?ko, Piotr,Kie?-Kononowicz, Katarzyna,Kuder, Kamil J.,Latacz, Gniewomir,Müller, Christa E.,Olejarz-Maciej, Agnieszka,Schabikowski, Jakub,Za?uski, Micha?

, (2020/04/20)

Annelated purinedione derivatives have b...

Separation and identification of an impurity from the istradefylline intermediate

Meng, Zihui,Wang, Hongyi,Wang, Yiyun,Xu, Haojie,Xu, Zhibin,Xue, Min,Zheng, Zhonghui

, p. 14493 - 14499 (2020/04/27)

Istradefylline is a selective adenosine ...

Improved synthesis technology of istradefylline

-

Paragraph 0013; 0014, (2018/04/28)

The invention provides an improved synth...

Inhibitory Effects of New Mercapto Xanthine Derivatives in Human mcf7 and k562 Cancer Cell Lines

Sultani, Haider N.,Ghazal, Rasha A.,Hayallah, Alaa M.,Abdulrahman, Loay K.,Abu-Hammour, Khaled,AbuHammad, Shatha,Taha, Mutasem O.,Zihlif, Malek A.

supporting information, p. 450 - 456 (2017/02/03)

A series of new 2-methyl-2-[(1,3-Diethyl...

52998-22-8 Process route

6-amino-1,3-diethyl-5-nitroso-1H,3H-pyrimidine-2,4-dione
89073-60-9

6-amino-1,3-diethyl-5-nitroso-1H,3H-pyrimidine-2,4-dione

5,6-diamino-1,3-diethyluracil
52998-22-8

5,6-diamino-1,3-diethyluracil

Conditions
Conditions Yield
With ammonium hydroxide; sodium dithionite; In water; for 0.5h;
98%
With sodium dithionite; ammonia; In water; at 60 ℃;
80%
With ammonium hydroxide; sodium dithionite; In water; at 60 ℃;
76%
6-amino-1,3-diethyl-5-nitroso-1H,3H-pyrimidine-2,4-dione; With ammonium hydroxide; at 70 ℃; for 0.5h;
With sodium dithionite; at 20 ℃; for 0.5h;
With sodium dithionite; ammonia; In water;
With hydrogen; In methanol; for 20h; Time;
6-amino-1,3-diethyl-5-nitroso-1H,3H-pyrimidine-2,4-dione; With potassium carbonate; In water; at 30 - 50 ℃;
With sodium dithionite; In water; at 20 ℃; for 1h;
With sodium dithionite; ammonia; In water; at 60 ℃; for 0.583333h;
With sodium dithionite;
With hydrogen; nickel; for 1h; under 3750.38 Torr;
6-amino-1,3-diethyluracil
41740-15-2

6-amino-1,3-diethyluracil

5,6-diamino-1,3-diethyluracil
52998-22-8

5,6-diamino-1,3-diethyluracil

Conditions
Conditions Yield
6-amino-1,3-diethyluracil; With nitric acid; acetic acid; In water;
With sodium dithionite; ammonia; In water; Further stages.;
80%
6-amino-1,3-diethyluracil; With nitric acid; acetic acid; In water; Inert atmosphere;
With sodium dithionite; ammonia; In water; Inert atmosphere;
80%
Multi-step reaction with 2 steps
1.1: aq. AcOH / 0.5 h / 75 °C
1.2: NaNO2 / 1 h / 20 °C
2.1: aq. NH3 / 0.5 h / 70 °C
2.2: Na2S2O4 / 0.5 h / 20 °C
With ammonium hydroxide; acetic acid;
Multi-step reaction with 2 steps
1: 74 percent / acetic acid; NaNO2 / H2O / 0.25 h / 50 - 60 °C
2: 80 percent / NH3; sodium dithionite / H2O / 60 °C
With sodium dithionite; ammonia; acetic acid; sodium nitrite; In water;
Multi-step reaction with 2 steps
1: sodium nitrite / acetic acid / 0.25 h / 50 - 60 °C
2: ammonium hydroxide; sodium dithionite / water / 0.5 h
With ammonium hydroxide; sodium dithionite; sodium nitrite; In water; acetic acid;
Multi-step reaction with 2 steps
1: cis-nitrous acid; acetic acid / water
2: sodium dithionite; ammonia / water
With sodium dithionite; ammonia; cis-nitrous acid; acetic acid; In water;
Multi-step reaction with 2 steps
1: sodium nitrite; acetic acid / 20 - 60 °C
2: ammonium hydroxide; sodium dithionite / water / 60 °C
With ammonium hydroxide; sodium dithionite; acetic acid; sodium nitrite; In water;
Multi-step reaction with 2 steps
1.1: acetic acid / 0.5 h
1.2: 1.5 h
2.1: hydrogen / methanol / 20 h
With hydrogen; acetic acid; In methanol;
Multi-step reaction with 2 steps
1: acetic acid; sodium nitrite / water / 2.5 h / 20 °C
2: sodium dithionite; ammonia / water / 0.58 h / 60 °C
With sodium dithionite; ammonia; acetic acid; sodium nitrite; In water;
Multi-step reaction with 2 steps
1: sodium nitrite / Acidic conditions
2: sodium dithionite
With sodium dithionite; sodium nitrite;
Multi-step reaction with 2 steps
1: sodium nitrite; acetic acid / 0.5 h / 60 °C
2: nickel; hydrogen / 1 h / 3750.38 Torr
With hydrogen; nickel; acetic acid; sodium nitrite;

52998-22-8 Upstream products

  • 89073-60-9
    89073-60-9

    6-amino-1,3-diethyl-5-nitroso-1H,3H-pyrimidine-2,4-dione

  • 623-76-7
    623-76-7

    N,N'-diethylurea

  • 41740-15-2
    41740-15-2

    6-amino-1,3-diethyluracil

  • 634-95-7
    634-95-7

    N,N-diethylurea

52998-22-8 Downstream products

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    142458-94-4

    6-amino-1,3-diethyl-5-<<(dicyclopropylmethyl)carbonyl>amino>uracil

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    (E)-8-(2,4-Dimethoxystyryl)-1,3-diethylxanthine

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    8-[(E)-2-(3,4-dimethoxyphenyl)ethenyl]-1,3-diethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione

  • 147700-39-8
    147700-39-8

    1,3-diethyl-8-(3,4,5-trimethoxy-styryl)-3,7-dihydro-purine-2,6-dione

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