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3-(4-nitro-phenyl)-1-phenyl-1H-indazole is a complex organic chemical compound with the molecular formula C21H14N4O2. It is characterized by a central indazole ring, which is fused to a phenyl group at the 1-position and another phenyl group at the 3-position. The phenyl group at the 3-position is further substituted with a nitro group at the para position. 3-(4-nitro-phenyl)-1-phenyl-1H-indazole is known for its potential applications in the field of medicinal chemistry, particularly as a precursor or intermediate in the synthesis of various biologically active molecules. Its structure and properties make it a subject of interest for researchers exploring new drug candidates and chemical entities with specific therapeutic potential.

1575-28-6

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1575-28-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1575-28-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1575-28:
(6*1)+(5*5)+(4*7)+(3*5)+(2*2)+(1*8)=86
86 % 10 = 6
So 1575-28-6 is a valid CAS Registry Number.

1575-28-6Downstream Products

1575-28-6Relevant academic research and scientific papers

Facile access to 1H-indazoles through iodobenzene-catalyzed C-H amination under mild, transition-metal-free conditions

Kashiwa, Mitsuhiro,Sonoda, Motohiro,Tanimori, Shinji

, p. 4720 - 4723 (2014)

The transition-metal- and halogen-free synthesis of N-aryl-substituted 1H-indazole and derivatives was accomplished on the basis of the iodobenzene-catalyzed intramolecular C-H amination of hydrazones under mild conditions. Reactions of hydrazones derived

An efficient transition-metal-free synthesis of 1H-indazoles from arylhydrazones with montmorillonite K-10 under O2 atmosphere

Yu, Jin,Lim, Jin Woo,Kim, Su Yeon,Kim, Jimin,Kim, Jae Nyoung

, p. 1432 - 1436 (2015/03/04)

An efficient transition-metal-free synthetic method of 1H-indazoles has been developed. The reaction of arylhydrazones in the presence of montmorillonite K-10 in 1,2-dichlorobenzene at 130 °C afforded 1H-indazoles in good yields most likely via a sequenti

Synthesis of 1 H-indazoles and 1 H-pyrazoles via FeBr3/O 2 mediated intramolecular C-H amination

Zhang, Tianshui,Bao, Weiliang

, p. 1317 - 1322 (2013/04/10)

A new synthesis of substituted 1H-indazoles and 1H-pyrazoles from arylhydrazones via FeBr3/O2 mediated C-H activation/C-N bond formation reactions is reported. The corresponding 1,3-diaryl-substituted indazoles and trisubstituted pyr

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