147724-85-4 Usage
Chemical structure
The compound consists of a benzofuran ring with a methoxy group at the 7-position and an ethylamine group attached to the benzofuran ring.
Molecular weight
Approximately 209.25 g/mol (calculated from the molecular formula)
Pharmacological properties
It is known for its potential as a serotonin receptor agonist.
Potential applications
The compound has been investigated for its possible use in the treatment of various conditions such as anxiety, depression, and neurodegenerative disorders.
Anti-inflammatory and antioxidant properties
It has shown promise in studies related to its potential as an anti-inflammatory and antioxidant agent.
Research and drug development
The compound is commonly used in research and drug development due to its pharmacological properties.
Ongoing research
Further research is ongoing to fully understand the potential applications and effects of 1-(7-methoxy-benzofuran-2-yl)-ethylamine.
Solubility
The solubility of the compound is not mentioned in the provided material, but it can be inferred that it may be soluble in organic solvents like methanol or ethanol, as is common for many organic compounds.
Stability
The stability of the compound is not explicitly mentioned in the material, but it is generally expected to be stable under normal laboratory conditions, as it is used in research and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 147724-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,7,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147724-85:
(8*1)+(7*4)+(6*7)+(5*7)+(4*2)+(3*4)+(2*8)+(1*5)=154
154 % 10 = 4
So 147724-85-4 is a valid CAS Registry Number.
147724-85-4Relevant academic research and scientific papers
Syntheses of 3-acetoacetylaminobenzo[b]furan derivatives having cysteinyl leukotriene 2 receptor antagonistic activity
Ando, Kumiko,Tsuji, Eriko,Ando, Yuko,Kuwata, Noriko,Kunitomo, Jun-Ichi,Yamashita, Masayuki,Ohta, Shunsaku,Kohno, Shigekatsu,Ohishi, Yoshitaka
, p. 625 - 635 (2007/10/03)
Novel 3-acetoacetylaminobenzo[b]furan derivatives having a modified triene system at the 3-position were synthesized starting with 3-aminobenzo[b]furans. The enol isomers, 3-[(3-hydroxybul-2-enonyl)amino]benzo[b]furans (1), of the 3-acetoacetylaminobenzo[b]furans were obtained as stable isomers owing to formation of a hydrogen bonding between the enol hydroxyl group and the amidocarbonyl group. The planarity of the C-2 substituent through the C-3 side chain suggested the existence of a modified conjugational triene system in the enol compound. Cysteinyl leukotriene 1 and 2 receptor antagonistic activities for these compounds were evaluated. 2-(4-Cyanobenzoyl or ethoxycarbonyl)-3-[(2-cyano-3-hydroxybut-2-enonyl)amino]benzo[e]furans (15g, 15o, 15u) were moderately active.
