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1H-Indole, 5-nitro-3-(4-nitrophenyl)-2-phenyl- is a complex organic compound with the molecular formula C21H14N4O5. It is a derivative of the indole structure, which is a heterocyclic aromatic organic compound. This specific compound features a 5-nitro group attached to the indole ring, a 4-nitrophenyl group at the 3-position, and a phenyl group at the 2-position. The presence of nitro groups and phenyl rings in this molecule contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. Due to its complex structure and multiple functional groups, 1H-Indole, 5-nitro-3-(4-nitrophenyl)-2-phenyl- may exhibit a range of reactivity and stability characteristics, making it an interesting subject for further chemical research and development.

1741-97-5

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1741-97-5 Usage

Molecular structure

1H-Indole, 5-nitro-3-(4-nitrophenyl)-2-phenylhas a complex molecular structure, which includes a core indole ring with various substituents.

Indole derivative

It is classified as an indole derivative, meaning it is a modified version of the parent compound indole.

Nitro group

The compound contains a nitro group (-NO2) on the 5th carbon atom of the indole ring, which may contribute to its reactivity and properties.

Additional substituents

Besides the nitro group, the molecule also has a 4-nitrophenyl group and a phenyl group attached to different positions, which can influence its aromaticity and reactivity.

Organic chemistry interest

1H-Indole, 5-nitro-3-(4-nitrophenyl)-2-phenylis of interest in the field of organic chemistry due to its unique structure and properties.

Potential applications

The compound may have potential applications in various industries, such as pharmaceuticals, agrochemicals, or materials science, due to its distinctive structure and properties.

Aromatic characteristics

The presence of nitro and phenyl groups suggests that the compound may possess aromatic characteristics, which can influence its chemical behavior and reactivity.

Reactive nature

The nitro and phenyl groups may also make the compound potentially reactive, making it an intriguing target for further study and the development of novel compounds with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1741-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1741-97:
(6*1)+(5*7)+(4*4)+(3*1)+(2*9)+(1*7)=85
85 % 10 = 5
So 1741-97-5 is a valid CAS Registry Number.

1741-97-5Upstream product

1741-97-5Relevant academic research and scientific papers

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