CAS 7013-41-4
:3-(3,3-dimethyl-1-phenyl-1,3-dihydro-2-benzofuran-1-yl)-N-methylpropan-1-amine hydrochloride (1:1)
Description:
3-(3,3-Dimethyl-1-phenyl-1,3-dihydro-2-benzofuran-1-yl)-N-methylpropan-1-amine hydrochloride, with the CAS number 7013-41-4, is a chemical compound that belongs to the class of substituted amphetamines. This substance features a complex structure that includes a benzofuran moiety, which contributes to its unique pharmacological properties. Typically, compounds of this nature may exhibit stimulant effects and can interact with neurotransmitter systems in the brain, particularly those involving dopamine and norepinephrine. The hydrochloride salt form indicates that it is a stable, water-soluble compound, which is often preferred for pharmaceutical applications due to improved bioavailability. As with many psychoactive substances, it is important to consider its potential for abuse and the regulatory status in various jurisdictions. Safety data, including toxicity and handling precautions, should be reviewed before any experimental use. Overall, this compound exemplifies the intricate relationship between chemical structure and biological activity in medicinal chemistry.
Formula:C20H26ClNO
InChI:InChI=1/C20H25NO.ClH/c1-19(2)17-12-7-8-13-18(17)20(22-19,14-9-15-21-3)16-10-5-4-6-11-16;/h4-8,10-13,21H,9,14-15H2,1-3H3;1H
SMILES:CC1(C)c2ccccc2C(CCCNC)(c2ccccc2)O1.Cl
Synonyms:- 1,3-Dihydro-N,3,3-trimethyl-1-phenyl-1-isobenzofuranpropanamine hydrochloride
- 1-isobenzofuranpropanamine, 1,3-dihydro-N,3,3-trimethyl-1-phenyl-, hydrochloride (1:1)
- 7013-41-4
- 3-(3,3-Dimethyl-1-phenyl-1,3-dihydro-2-benzofuran-1-yl)-N-methylpropan-1-amine hydrochloride (1:1)
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Found 2 products.
Talopram hydrochloride
CAS:<p>Talopram hydrochloride is an antiviral drug that inhibits the enzyme phospholipase A2 and the viral enzyme protease. It is used to treat a variety of nervous system disorders, including Parkinson's disease and Alzheimer's disease, as well as certain cancers. The mechanism of action of Talopram hydrochloride is not fully known, but it may be due to its inhibition of phospholipases and proteases in the body. This drug interacts with polymorphic variants in some individuals, affecting bioavailability and metabolization. It also interacts with other drugs by forming conjugates or being transformed into metabolites that are more polar than the original molecule. In addition, this drug can cause liver disorders when taken with other drugs that are processed by the liver.</p>Formula:C20H26ClNOPurity:Min. 95%Molecular weight:331.9 g/molTalopram hydrochloride
CAS:<p>noradrenalin transporter (NET) inhibitor</p>Formula:C20H26ClNOPurity:98%Color and Shape:SolidMolecular weight:331.88

