29636-94-0

Basic information

• Product Name: 3H-Indolium, 1-(2-hydroxyethyl)-2,3,3-trimethyl-, bromide
• CAS NO: 29636-94-0
• Molecular Formula: C13H18NO.Br
• Molecular Weight: 284.196
• Mol File: 29636-94-0.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: 3H-Indolium, 1-(2-hydroxyethyl)-2,3,3-trimethyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Indolium, 1-(2-hydroxyethyl)-2,3,3-trimethyl-, bromide(29636-94-0)
• EPA Substance Registry System: 3H-Indolium, 1-(2-hydroxyethyl)-2,3,3-trimethyl-, bromide(29636-94-0)

Safety Data

• Hazardous Substances Data: 29636-94-0(Hazardous Substances Data)

Usage

General Description

3H-Indolium, 1-(2-hydroxyethyl)-2,3,3-trimethyl-, bromide is a chemical compound with the formula C13H18BrNO. It is a bromide salt of a highly substituted indolium cation, which is a type of heterocyclic organic compound. 3H-Indolium, 1-(2-hydroxyethyl)-2,3,3-trimethyl-, bromide is often used in organic synthesis and chemical research as a reagent for various reactions. It can also be used as a dye in the textile industry and as a stain in biological research. Additionally, it has been studied for potential pharmaceutical applications due to its unique chemical structure and properties.

Upstream product

• 1640-39-7 2,3,3-trimethylindoleniune 
• 540-51-2 2-bromoethanol 
• 54683-96-4 2,3,3-Trimethyl-indolenin 
• 563-80-4 3-methyl-butan-2-one 
• 100-63-0 phenylhydrazine 

Downstream Products

• 59335-14-7 10-[2-(4-dimethylaminophenyl)ethylene]-9,9-trimethyl-indolino-[2,1-b]oxazolidine 
• 16111-07-2 2-(3',3'-dimethyl-6-nitro-3'H-spiro[chromene-2,2'-indol]-1'-yl)-ethanol 
• 25952-50-5 1-(β-methacryloxyethyl)-3,3-dimethyl-6'-nitrospiro(indoline-2,2'-<2H>benzopyran) 

Relevant articles and documents

Application of stimuli-responsive FRET behavior toward cyanide detection in a photo-switchable [2]pseudorotaxane polymer containing the BODIPY donor and the merocyanine acceptor

We have developed a supramolecular (close form) [2]pseudorotaxane polymer containing the green-emissive (λem= 523 nm) BODIPY-based pillar[5]arene host and the non-emissive spiropyran (SP)-based cyano guest (close form), which can be converted t

Unlocking Chemically Encrypted Information Using Three Types of External Stimuli

Encryption is critical to information security; however, existing chemical-based information encryption strategies are still in their infancy. We report here a new approach to chemical encryption involving a supramolecular gel QR (quick response) code wit

Light-Driven Expansion of Spiropyran Hydrogels

The incorporation of molecular switches in organic structures is of great interest in the chemical design of stimuli-responsive materials that mimic the complex functions of living systems. Merocyanine dyes that convert to spiropyran moieties upon exposure to visible light have been extensively studied as they can be incorporated in hydrated covalent networks that will expel water when this conversion occurs and induce a volumetric shrinkage. We report here on a sulfonate-based water-soluble photoswitch that, in contrast to the well-known systems, triggers a volumetric expansion in hydrogels upon exposure to photons. Contraction is in turn observed under dark conditions in a highly reversible manner. The novel behavior of the photoswitch incorporated in the covalent network was predicted by coarse-grained simulations of the system's chemical structure. Using pH control and polymeric structures that differ in lower critical solution temperature, we were able to develop hydrogels with highly tunable volumetric expansion. The novel molecular function of the systems developed here led to materials with the negative phototaxis observed in plants and could expand the potential use of hydrogels as sensors, soft robots, and actuators.