179898-22-7

Basic information

• Product Name: 2,2,4-triMethyl-1,2-dihydroquinolin-7-ol
• Synonyms: 2,2,4-triMethyl-1,2-dihydroquinolin-7-ol;2,2,4-trimethyl-1H-quinolin-7-ol
• CAS NO: 179898-22-7
• Molecular Formula: C₁₂H₁₅NO
• Molecular Weight: 189.2536
• Mol File: 179898-22-7.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,2,4-triMethyl-1,2-dihydroquinolin-7-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,4-triMethyl-1,2-dihydroquinolin-7-ol(179898-22-7)
• EPA Substance Registry System: 2,2,4-triMethyl-1,2-dihydroquinolin-7-ol(179898-22-7)

Safety Data

• Hazardous Substances Data: 179898-22-7(Hazardous Substances Data)

Usage

Derived from

Quinoline

Uses

Antioxidant and stabilizer in the food industry
+ Prevents oxidation of food products, extending shelf life and preserving color and flavor
+ Used in the production of rubber and plastics to prevent degradation from heat and oxygen exposure

Pharmaceutical potential

Possible treatment for conditions such as Alzheimer's disease and as an anti-inflammatory agent

Upstream product

• 591-27-5 m-Hydroxyaniline 
• 74-99-7 prop-1-yne 
• 179897-97-3 1,2-dihydro-2,2,4-trimethyl-7-(1,1,1-trimethylacetoxy)quinoline 
• 67-64-1 acetone 
• 1810-74-8 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline 
• 536-90-3 m-Anisidine 

Downstream Products

• 179898-71-6 2-bromo-N-(2-methyl-2-propenyl)-5-nitroaniline 
• 91-22-5 quinoline 
• 179899-10-6 (R/S)-1,2,3,4-Tetrahydro-4-methyl-7-methoxyquinoline 
• 179899-02-6 (R/S)-3-ethyl-1,2,3,4-tetrahydro-2,2-dimethyl-4-quinolinone 
• 580-19-8 quinolin-7-ylamine 
• 41148-72-5 2,2,4-trimethyl-1,2-dihydro-quinolin-7-ylamine 
• 18791-99-6 4-bromo-2-thiophenecarbonitrile 
• 179898-00-1 1-tert-butyloxycarbonyl-1,2,3,4-tetrahydro-4-quinolinone 
• 1441383-55-6 C₄₈H₃₇F₂₆N₂O₃⁽¹⁺⁾*Cl^(1-) 

Relevant articles and documents

Real time observation of microwave-enhanced reactions via fast FTIR spectroscopy

Microwave-enhanced reactions are very fast in comparison to thermal reactions. The determination of optimal end point often fails because conventional analytical methods are too slow. Therefore, we established a fast method using FTIR spectroscopy. The re

ASYMMETRIC RHODAMINE DYE AND USE THEREOF IN BIOLOGICAL ASSAYS

The present disclosure relates to N-protected NH-rhodamine dyes and their use in nucleic acid detection. In particular, the disclosure relates to methods of making N-protected NH-rhodamine dyes, and methods of use of N-protected NH-rhodamine dyes (e.g., human identification). Certain dyes provided herein have unique spectral properties that complement those in existing dye sets and can be used to expand the number of reporter dyes that can be included for HID applications and other biological assays. Those fluorescent compounds are useful to label synthetic oligonucleotides. Formula (I).

Rhodamine F: A novel class of fluorous ponytailed dyes for bioconjugation

Incorporation of fluorous ponytails such as polyfluorinated alkyl residues (CH2)m(CF2)nCF3 leads to a novel class of bright rhodamine-based fluorescence dyes. These dyes combine the excellent photophysical properties of the frequently used rhodamine dyes with the unique features of "light" fluorous molecules. One of those features is the possibility to separate substances utilizing fluorous solid-phase extraction (F-SPE), which is based on the specific intermolecular interaction between fluorous compounds. Thus, molecules, which are labeled with these new dyes, are not only accessible to fluorescence experiments, but can also be easily purified (via so-called FluoroFlash columns) prior to use. The dyes were bound to a cell penetrating peptoid (polycationic oligo(N-substituted) glycine) on solid supports. These conjugates were purified with F-SPE before their photophysical and biological properties were investigated. The Royal Society of Chemistry 2013.