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5-AMINOINDAZOLE

CAS No.: 19335-11-6

product details:

Purity: 99%

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Quality manufacturer supply 5-AMINOINDAZOLE 19335-11-6 in stock with high standard

  • Molecular Formula: C7H7N3
  • Molecular Weight: 133.153
  • Appearance/Colour: white to light yellow crystal powder 
  • Vapor Pressure: 5.92E-10mmHg at 25°C 
  • Melting Point: 175-178 °C 
  • Refractive Index: 1.806 
  • Boiling Point: 376.609 °C at 760 mmHg 
  • PKA: 14.52±0.40(Predicted) 
  • Flash Point: 209.521 °C 
  • PSA: 54.70000 
  • Density: 1.367 g/cm3 
  • LogP: 1.72630 

5-AMINOINDAZOLE(Cas 19335-11-6) Usage

Application

1H-Indazol-5-amine is a useful research chemical, an indazole derivatives with anti- inflammatory properties.

InChI:InChI=1/C6H6N4/c7-4-1-5-6(8-2-4)10-3-9-5/h1-3H,7H2,(H,8,9,10)

19335-11-6 Relevant articles

Design, synthesis and biological evaluation of indazole-pyrimidine based derivatives as anticancer agents with anti-angiogenic and antiproliferative activities

Elsayed, Nevine M. Y.,Abou El Ella, Dalal A.,Serya, Rabah A. T.,Tolba, Mai F.,Shalaby, Raed,Abouzid, Khaled A. M.

, p. 881 - 899 (2016)

Three series of novel indazole-pyrimidin...

Design, synthesis, biological evaluation and dynamics simulation of indazole derivatives with antiangiogenic and antiproliferative anticancer activity

Elsayed, Nevine M.Y.,Serya, Rabah A.T.,Tolba, Mai F.,Ahmed, Marawan,Barakat, Khaled,Abou El Ella, Dalal A.,Abouzid, Khaled A.M.

, p. 340 - 359 (2019)

VEGFR-2 has a pivotal role in promoting ...

Design, synthesis, and biological evaluation of new B-RafV600E kinase inhibitors

Wang, Peng-Fei,Zhang, Yong-Jiao,Wang, Dong,Hu, Hui-Min,Wang, Zhong-Chang,Xu, Chen,Qiu, Han-Yue,Zhu, Hai-Liang

, p. 2372 - 2380 (2018)

The association of deregulated signal pa...

PYRROLIDINYL-BASED COMPOUNDS

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Paragraph 0137, (2021/04/10)

Disclosed herein are pyrrolidinyl-based ...

COMPOUND SERVING AS IRAK INHIBITOR

-

Paragraph 0199-0200, (2021/10/07)

The present disclosure relates a compoun...

2-pyridine substituted urea structural small molecule compounds as well as synthesis and application thereof

-

Paragraph 0197; 0298-0300, (2020/03/03)

The invention relates to 2-pyridine subs...

Discovery of 1-(1H-indazol-4-yl)-3-((1-phenyl-1H-pyrazol-5-yl)methyl) ureas as potent and thermoneutral TRPV1 antagonists

Kang, Jin Mi,Kwon, Sun Ok,Ann, Jihyae,Blumberg, Peter M.,Ha, Heejin,Yoo, Young Dong,Frank-Foltyn, Robert,Lesch, Bernhard,Bahrenberg, Gregor,Stockhausen, Hannelore,Christoph, Thomas,Lee, Jeewoo

, (2020/10/06)

A series of 1-indazol-3-(1-phenylpyrazol...

19335-11-6 Process route

5-nitroindazole
5401-94-5

5-nitroindazole

1H-indazol-5-ylamine
19335-11-6

1H-indazol-5-ylamine

Conditions
Conditions Yield
With hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; at 25 ℃; Autoclave; Inert atmosphere;
100%
With hydrogen; palladium 10% on activated carbon; In methanol; under 760.051 Torr;
97%
With hydrogen; palladium 10% on activated carbon; In methanol; under 1551.49 Torr;
97%
With palladium 10% on activated carbon; hydrogen; In methanol; under 1551.49 Torr;
97%
With palladium 10% on activated carbon; hydrogen; In methanol; at 40 ℃; under 1551.49 Torr;
97%
With palladium 10% on activated carbon; hydrogen; In methanol; at 40 ℃; for 3h; under 1551.49 Torr;
97.2%
With hydrazine; palladium on activated charcoal; In methanol; Heating;
90%
With potassium tert-butylate; isopropyl alcohol; bis(pinacol)diborane; at 110 ℃; for 2h;
88%
With palladium on activated charcoal; hydrogen; In methanol; for 12h;
88%
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 2h;
65%
With ammonium hydroxide; iron(II) sulfate;
With hydrogenchloride; zinc;
With nickel; Hydrogenation;
With hydrogenchloride; palladium dihydroxide; In methanol;
With iron; acetic acid;
With iron; ammonium chloride; In ethanol; water; for 2h; Reflux;
With palladium 10% on activated carbon; hydrazine hydrate; In ethanol; for 0.166667h; Reflux;
With palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 20 ℃; for 1.5h;
With palladium 10% on activated carbon; hydrogen; In methanol;
190.6 mg
With palladium on activated charcoal; hydrogen; In methanol; at 20 ℃;
With palladium on activated carbon; hydrogen; In methanol; at 20 ℃; for 16h;
5-nitroindazole
5401-94-5

5-nitroindazole

5-amuio-1H-indazole

5-amuio-1H-indazole

1H-indazol-5-ylamine
19335-11-6

1H-indazol-5-ylamine

Conditions
Conditions Yield
carbon palladium; In methanol;
100%

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    (1H-Indazol-5-yl)-(1-phenethyl-piperidin-4-ylidene)-amine

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    C15 H14 N4 O3 S

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