CAS 10553-11-4

4-Nitroindole-3-carboxaldehyde

Description:

4-Nitroindole-3-carboxaldehyde is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a nitro group (-NO2) at the 4-position and an aldehyde group (-CHO) at the 3-position of the indole ring significantly influences its chemical properties and reactivity. This compound typically appears as a yellow to orange solid and is soluble in organic solvents. It is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, such as nucleophilic additions and condensation reactions. The nitro group can also serve as a site for further functionalization, making it a versatile intermediate in synthetic chemistry. Additionally, 4-Nitroindole-3-carboxaldehyde may exhibit biological activity, which warrants further investigation for its potential therapeutic uses. Safety precautions should be taken when handling this compound, as nitro compounds can be hazardous.

Formula: C₉H₆N₂O₃

InChI: InChI=1/C9H6N2O3/c12-5-6-4-10-7-2-1-3-8(9(6)7)11(13)14/h1-5,10H

SMILES: c1cc2c(c(c[nH]2)C=O)c(c1)N(=O)=O

Synonyms:

• 3-Formyl-4-nitroindole
• 4-nitro-1H-indole-3-carbaldehyde

4-Nitroindole-3-carboxaldehyde, 96%

CAS: 10553-11-4

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Formula: C₉H₆N₂O₃

Purity: 96%

Molecular weight: 190.16

Ref: 02-H63595

4-Nitroindole-3-carboxaldehyde

CAS: 10553-11-4

Formula: C₉H₆N₂O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 190.1555

Ref: IN-DA003LVH

4-Nitroindole-3-carboxaldehyde

CAS: 10553-11-4

4-Nitroindole-3-carboxaldehyde

Purity: 97%

Molecular weight: 190.16g/mol

Ref: 54-OR923916

4-NITRO-1H-INDOLE-3-CARBALDEHYDE

CAS: 10553-11-4

Formula: C₉H₆N₂O₃

Purity: 98%

Molecular weight: 190.158

Ref: 10-F304801