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(3-fluoro-phenyl)-(4-nitro-phenyl)-amine is an organic compound characterized by its unique molecular structure, which consists of two phenyl rings connected through an amine group. One of the phenyl rings is substituted with a fluorine atom at the 3rd position, while the other is substituted with a nitro group at the 4th position. (3-fluoro-phenyl)-(4-nitro-phenyl)-amine is known for its potential applications in the pharmaceutical industry, particularly in the development of drugs targeting various diseases. Its chemical properties, such as reactivity and stability, are influenced by the presence of the electron-withdrawing fluorine and nitro groups, which can affect its interactions with other molecules and its overall behavior in chemical reactions.

330-86-9

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330-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330-86-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 330-86:
(5*3)+(4*3)+(3*0)+(2*8)+(1*6)=49
49 % 10 = 9
So 330-86-9 is a valid CAS Registry Number.

330-86-9Downstream Products

330-86-9Relevant academic research and scientific papers

Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines

Akram, Manjur O.,Das, Avishek,Chakrabarty, Indradweep,Patil, Nitin T.

, p. 8101 - 8105 (2019)

The first example of ancillary (P,N)-ligand-enabled gold-catalyzed C-N cross-coupling reactions of aryl iodides with amines is reported. The high generality of the reaction in de novo synthesis, late-stage modifications, and cascade processes to access functionalized indolinones and carbazoles underscores the synthetic potential of the presented strategy. Monitoring the reaction with ESI-HRMS and NMR provided strong evidence for the in situ formation of putative high valent Au(III) intermediates.

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