2426-62-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(Benzyloxy)-3-Methoxy-β,6-dinitrostyrene is used as an intermediate in the synthesis of 4-Hydroxymelatonin (H944635), a metabolite of Melatonin (M215000). Melatonin is a hormone found in animals that plays a vital role in regulating the sleep-wake cycle. The compound is utilized for its potential therapeutic applications in treating sleep disorders and other conditions related to the circadian rhythm.
Additionally, due to its reactivity and structural features, 2-(Benzyloxy)-3-Methoxy-β,6-dinitrostyrene can be further modified and used in the development of other bioactive molecules with potential applications in various therapeutic areas, such as oncology, neurology, and cardiovascular diseases.
Used in Chemical Industry:
In the chemical industry, 2-(Benzyloxy)-3-Methoxy-β,6-dinitrostyrene can be employed as a building block for the synthesis of a wide range of specialty chemicals, including dyes, pigments, and polymers. Its unique structural features allow for various chemical reactions, such as reduction, substitution, and coupling, which can lead to the formation of novel compounds with specific properties and applications.
Furthermore, the compound's reactivity and structural diversity make it a valuable tool for research and development in the field of organic chemistry, where it can be used to explore new reaction pathways and develop innovative synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 2426-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2426-62:
(6*2)+(5*4)+(4*2)+(3*6)+(2*6)+(1*2)=72
72 % 10 = 2
So 2426-62-2 is a valid CAS Registry Number.
2426-62-2Relevant academic research and scientific papers
Synthesis and adrenolytic activity of 1-(1H-indol-4-yloxy)-3-(2-(2-methoxy phenoxy)ethylamino)propan-2-ol analogs and its enantiomers. Part 2
Groszek, Grazyna,Nowak-Krol, Agnieszka,Wdowik, Tomasz,Swierczynski, Dariusz,Bednarski, Marek,Otto, Monika,Walczak, Maria,Filipek, Barbara
experimental part, p. 5103 - 5111 (2010/02/28)
The synthesis of (2RS)-1-(5-methoxy-1H-indol-4-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol and (2RS)-1-(7-methoxy-1H-indol-4-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol and its enantiomers, analogs of 1-(1H-indol-4-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol ((RS)-9) is described. Compounds were tested for electrographic, antiarrhythmic, hypotensive and spasmolytic activities as well as for α1-, α2- and β1-adrenoceptors binding affinities. The antagonist potency of the new compounds was compared with carvedilol and (RS)-9.
