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2-Methyl-2H-indazol-5-amine

Detailed Information

  • Product Name:2-Methyl-2H-indazol-5-amine
  • CasNo.:60518-59-4
  • MF:C8H9 N3
  • MW:147.18

pd_nature

  • Purity:99%
  • pd_boiling:125
  • Packing:
  • Throughput:

Product Details;

CasNo: 60518-59-4

MF: C8H9 N3

Buy Quality 2-Methyl-2H-indazol-5-amine 60518-59-4 In Stock with Immediately Delivery

  • Molecular Formula:C8H9 N3
  • Molecular Weight:147.18
  • Vapor Pressure:3.26E-05mmHg at 25°C 
  • Melting Point:125 
  • Boiling Point:354.8°C at 760 mmHg 
  • PKA:3.65±0.10(Predicted) 
  • Flash Point:168.4°C 
  • PSA:43.84000 
  • Density:1.27g/cm3 
  • LogP:1.73670 

2-METHYL-2H-INDAZOL-5-AMINE(Cas 60518-59-4) Usage

General Description

2-Methyl-2H-indazol-5-amine is a chemical compound with the molecular formula C8H9N3. It is a derivative of indazole, a heterocyclic compound containing a benzene ring fused to a five-membered nitrogen-containing ring. 2-Methyl-2H-indazol-5-amine has potential application in pharmaceutical and medicinal chemistry, possibly in the development of new drugs or as a precursor in organic synthesis. Its specific properties and potential uses would depend on further research and development in the field of chemistry and pharmacology.

InChI:InChI=1/C8H9N3/c1-11-5-6-4-7(9)2-3-8(6)10-11/h2-5H,9H2,1H3

60518-59-4 Relevant articles

INHIBITORS OF LYSINE SPECIFIC DEMETHYLASE-1

-

Paragraph 00146, (2016/01/25)

The present invention relates generally ...

Unparalleled Ease of Access to a Library of Biheteroaryl Fluorophores via Oxidative Cross-Coupling Reactions: Discovery of Photostable NIR Probe for Mitochondria

Cheng, Yangyang,Li, Gaocan,Liu, Yang,Shi, Yang,Gao, Ge,Wu, Di,Lan, Jingbo,You, Jingsong

supporting information, p. 4730 - 4738 (2016/05/09)

The development of straightforward acces...

HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES

-

Paragraph 000410, (2016/05/02)

Described herein are compounds of Formul...

2,4-Pyrimidinediamine Compounds and Their Uses

-

Paragraph 0525; 0538, (2015/11/10)

The present invention provides 2,4-pyrim...

60518-59-4 Process route

2-methyl-5-nitro-2H-indazole
5228-48-8

2-methyl-5-nitro-2H-indazole

5-amino-2-methyl-2H-indazole
60518-59-4

5-amino-2-methyl-2H-indazole

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In methanol; dichloromethane; at 50 ℃; under 2250.23 Torr;
98%
With palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane; at 50 ℃; for 3h; under 2585.81 Torr;
85%
With hydrogen; palladium; In ethanol; under 836 Torr;
80%
With 3% Pd/C; hydrogen; In methanol; dichloromethane; at 50 ℃; for 6h; under 18751.9 Torr;
With iron; ammonium chloride; In ethanol; water; for 2h; Reflux;
5-nitroindazole
5401-94-5

5-nitroindazole

5-amino-2-methyl-2H-indazole
60518-59-4

5-amino-2-methyl-2H-indazole

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: 44 percent / KOH; water / 0.5 h / 75 °C
2: 20 percent / conc. HCl; SnCl2*H2O / methanol / Heating
With hydrogenchloride; potassium hydroxide; water; tin(ll) chloride; In methanol;
Multi-step reaction with 2 steps
1: 44 percent / KOH; water / 0.5 h / 75 °C
2: 98 percent / H2 / Pd/C / methanol; CH2Cl2 / 50 °C / 2250.23 Torr
With potassium hydroxide; water; hydrogen; palladium on activated charcoal; In methanol; dichloromethane;
Multi-step reaction with 2 steps
1: 43 percent / potassium hydroxide / H2O / 45 °C
2: 80 percent / H2, buffer (pH = 7) / 10percent Pd / ethanol / 836 Torr
With potassium hydroxide; hydrogen; palladium; In ethanol; water;
Multi-step reaction with 2 steps
1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C
2: ammonium chloride; iron / water; ethanol / 2 h / Reflux
With iron; sodium hydride; ammonium chloride; In ethanol; water; N,N-dimethyl-formamide;

60518-59-4 Upstream products

  • 5228-48-8
    5228-48-8

    2-methyl-5-nitro-2H-indazole

  • 5401-94-5
    5401-94-5

    5-nitroindazole

  • 65750-01-8
    65750-01-8

    5-nitro-2H-indazole

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