52607-60-0

Usage

Chemical structure

A spirooxindole compound with a spiro-structured chromene ring system, characterized by an indole group fused to a chromene ring.

Substituents

Contains three methyl groups at the 1', 3', and 3' positions, and a diazenyl group with a 4-nitrophenyl substituent at the 6-position.

Family

Belongs to the spirochromene family of compounds.

Potential applications

Has potential applications in various fields, including pharmaceuticals, materials science, and organic synthesis.

Unique structural properties

The compound's unique structural properties contribute to its potential for various applications.

Biological activities

The compound may have potential biological activities, but further research is needed to fully understand its properties and potential uses.

Research status

Further research is required to fully understand the properties and potential uses of 1',3',3'-trimethyl-6-((4-nitrophenyl)diazenyl)spiro[chromene-2,2'-indoline].

Molecular weight

The molecular weight of the compound is not provided in the material, but it can be calculated once the complete chemical formula is known.

Physical properties

The physical properties of the compound, such as melting point, boiling point, solubility, and appearance, are not provided in the material and would require further investigation.

Upstream product

• 90-02-8 salicylaldehyde 
• 100-05-0 4-nitrobenzenediazonium chloride 
• 118-12-7 1,3,3-Trimethyl-2-methyleneindoline 
• 32041-64-8 5-(4-nitrophenylazo)salicylaldehyde 

Relevant academic research and scientific papers

Spiropyran-azobenzene-DBU system as solvent indicator

A dyad bearing azobenzene and spiropyran units was synthesized and its applications in indicating the polarity and protic or aprotic properties of a solvent were explored. The spiropyran-azobenzene derivative (SPAB) can be induced to different forms in different miscellaneous solvents accompanied with different color changes and spectral characteristics at the presence of organic base DBU. In a nonpolar or low-polar solvent, SPAB exists in thermostable spiropyran form with yellow color output. While in an aprotic polar solvent, the spiropyran part isomerized to merocyanine form giving a blue color. When SPAB is subjected to a protic solvent, the alkylation reaction occurs at the oxygen generating the alkylated-SPAB with red color. This solvent-dependent property can be used for discriminating solvent type.

Thermo- and Photochromic Dyes: Spiro(indolinebenzopyrans) 2. - Detailed Assignment of the 1H NMR Spectra and Structural Aspects of the Closed Form of 1,3,3-Trimethylspiro(indoline-2,2'-benzopyrans)

The proton NMR assignments for a series of 12 thermo- and photochromic 1,3,3-trimethylspiro(indoline-2,2'-benzopyrans) dyes is reported.All of the protons in the dye molecule were assigned through a combination of homonuclear decoupling experiments and correlation spectroscopy.The relative stereochemistry of the indolino gem-dimethyl groups was assigned so that, for the S-epimer, the pro-R methyl was found to resonate at 1.24 ppm while the pro-S methyl appeared at 1.37 ppm for compound 1. KEY WORDS: Thermo- and photochromic dyes, Spiro(indoline-2,2'-benzopyrans), 1H NMR assignments