CAS 99473-14-0
:(5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid
Description:
(5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid is a complex organic compound characterized by its unique structural features, including a hepten-3-ynoic acid backbone with multiple substituents. The presence of a dimethyl group and a naphthalenylmethyl amino group contributes to its distinctive chemical properties. This compound is likely to exhibit both hydrophobic and hydrophilic characteristics due to the combination of its aliphatic and aromatic components. The triple bond in the hepten-3-ynoic acid portion suggests potential reactivity, particularly in addition reactions. Additionally, the presence of the amino group may impart basicity and enable interactions with various biological systems, potentially influencing its pharmacological properties. The compound's structure suggests it may be of interest in medicinal chemistry or as a synthetic intermediate in organic synthesis. However, specific biological activity, solubility, and stability would require further investigation through empirical studies.
Formula:C21H23NO2
InChI:InChI=1S/C21H23NO2/c1-21(2,20(23)24)14-7-4-8-15-22(3)16-18-12-9-11-17-10-5-6-13-19(17)18/h4-6,8-13H,15-16H2,1-3H3,(H,23,24)/b8-4+
InChI key:InChIKey=DSPCPJFHUUUMEV-XBXARRHUSA-N
SMILES:C(N(C/C=C/C#CC(C(O)=O)(C)C)C)C=1C2=C(C=CC1)C=CC=C2
Synonyms:- 5-Hepten-3-ynoic acid, 2,2-dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-, (E)-
- (5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid
- Carboxyterbinafine
- Carboxyterbinafiine
- 5-Hepten-3-ynoic acid, 2,2-dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-, (5E)-
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Found 4 products.
(5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid
CAS:(5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid is a drug product that has been custom synthesized. It is available in high purity (>98%) and with analytical data. This chemical is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. (5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid has been shown to have pharmacological activity on the central nervous system and may be used as an antidepressant drug candidate.Formula:C21H23NO2Purity:Min. 95%Molecular weight:321.41 g/mol



