Cas no 25487-28-9 (Talsupram Hydrochloride)

Talsupram Hydrochloride is a selective serotonin reuptake inhibitor (SSRI) with potential applications in neurological and psychiatric research. Its high affinity for the serotonin transporter (SERT) makes it a valuable tool for studying serotonin-mediated neurotransmission and related disorders. The hydrochloride salt form ensures improved solubility and stability, facilitating experimental use in vitro and in vivo. Talsupram Hydrochloride exhibits minimal off-target activity, enhancing its specificity in mechanistic studies. Researchers utilize it to explore depression, anxiety, and other serotonin-linked conditions. Its well-characterized pharmacological profile supports reproducibility in preclinical investigations. The compound is typically supplied as a high-purity reference standard, ensuring reliable results in biochemical assays and neuropharmacological studies.
Talsupram Hydrochloride structure
Talsupram Hydrochloride structure
Product Name:Talsupram Hydrochloride
CAS No:25487-28-9
MF:C20H26ClNS
MW:347.945143222809
CID:262498
PubChem ID:69889594
Update Time:2025-05-22

Talsupram Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • Benzo[c]thiophene-1-propanamine,1,3-dihydro-N,3,3-trimethyl-1-phenyl-, hydrochloride (1:1)
    • 3-(3,3-dimethyl-1-phenyl-2-benzothiophen-1-yl)propyl-methylazanium,chloride
    • Talsupram hydrochloride
    • 1,3-Dihydro-1,1-dimethyl-3-(3-methylaminopropyl)-3-phenylbenzo(c)thiophen hydrochlorid
    • 1,3-Dihydro-1-phenyl-N,3,3-trimethylbenzo(c)thiophene-1-propylamine hydrochloride
    • AC1L1OUB
    • AC1Q1SQX
    • Benzo(c)thiophene-1-propylamine, 1,3-dihydro-1-phenyl-N,3,3-trimethyl-, hydrochloride
    • C20H25
    • LU 5-005 hydrochloride
    • N-Methyl-3-(3,3-dimethyl-1-phenyl-1,3-dihydrobenzo(c)thiophen-1-yl)propylamin hydrochlorid
    • Talsupram HCl
    • 1-(3-methylaminopropyl)-1-phenyl-3,3-dimethylthiophthalane hydrochloride
    • Benzo[c]thiophene-1-propanamine, 1,3-dihydro-N,3,3-trimethyl-1-phenyl-, hydrochloride
    • 3-(3,3-Dimethyl-1-phenyl-1,3-dihydro-2-benzothiophen-1-yl)-N-methylpropan-1-amine--hydrogen chloride (1/1)
    • T3HY6R3E6V
    • 3-(3,3-Dimethyl-1-phenyl-1,3-dihydrobenzo[c]thiophen-1-yl)-N-methylpropan-1-aminehydrochloride
    • CS-0025309
    • N,3,3-Trimethyl-1-phenyl-1-benzo[c]thiophenepropylamine hydrochloride
    • 3-(3,3-dimethyl-1-phenyl-2-benzothiophen-1-yl)-N-methylpropan-1-amine;hydrochloride
    • AKOS024458111
    • HY-103218
    • 3-(3, 3-dimethyl-1-phenyl-2-benzothiophen-1-yl)-N-methylpropan-1-amine;hydrochloride
    • Benzo[c]thiophene-1-propanamine, 1,3-dihydro-N,3,3-trimethyl-1-phenyl-, hydrochloride (1:1)
    • 3-(3,3-Dimethyl-1-phenyl-1,3-dihydrobenzo[c]thiophen-1-yl)-N-methylpropan-1-amine hydrochloride
    • 1,3-Dihydro-N,3,3-trimethyl-1-phenylbenzo[c]thiophene-1-propanamine hydrochloride
    • Talsupram (hydrochloride)
    • 25487-28-9
    • DTXSID60948373
    • 3-(3,3-dimethyl-1-phenyl-2-benzothiophen-1-yl)-N-methylpropan-1-amine hydrochloride
    • Lu 5-005
    • GLXC-03076
    • Talsupram Hydrochloride
    • Inchi: 1S/C20H25NS.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
    • InChI Key: YMZCMCDSCRSIBS-UHFFFAOYSA-N
    • SMILES: Cl.S1C(C)(C)C2C=CC=CC=2C1(C1C=CC=CC=1)CCCNC

Computed Properties

  • Exact Mass: 347.147
  • Monoisotopic Mass: 347.147
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 5
  • Complexity: 361
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 37.3A^2

Experimental Properties

  • Density: 1.043
  • Boiling Point: 427.6°Cat760mmHg
  • Flash Point: 212.4°C

Talsupram Hydrochloride Pricemore >>

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Additional information on Talsupram Hydrochloride

Talsupram Hydrochloride: A Comprehensive Overview

Talsupram Hydrochloride, also known by its CAS number 25487-28-9, is a compound that has garnered significant attention in the fields of pharmacology and chemistry due to its unique properties and potential applications. This compound, which belongs to the class of hydrochlorides, has been extensively studied for its role in various biological systems. Recent advancements in research have shed light on its mechanisms of action, pharmacokinetics, and therapeutic potential, making it a subject of interest for both academic and industrial researchers.

The chemical structure of Talsupram Hydrochloride is characterized by a complex arrangement of functional groups that contribute to its biological activity. Its molecular formula and molecular weight have been precisely determined, providing a foundation for understanding its interactions with cellular components. The compound's solubility properties, particularly in aqueous solutions, are crucial for its formulation and delivery in pharmaceutical applications. Researchers have explored various methods to optimize these properties, ensuring that Talsupram Hydrochloride can be effectively utilized in therapeutic settings.

In terms of pharmacology, Talsupram Hydrochloride has demonstrated promising effects in preclinical studies. Its ability to modulate specific cellular pathways has been extensively investigated, with recent studies highlighting its potential as a therapeutic agent in the treatment of neurological disorders. The compound's bioavailability and metabolism have also been studied in detail, providing insights into its pharmacokinetic profile. These findings are essential for determining the appropriate dosing regimens and administration routes for clinical use.

The application of Talsupram Hydrochloride extends beyond pharmacology, with researchers exploring its role in diagnostic tools and imaging techniques. Its ability to interact with specific biomarkers has opened new avenues for early disease detection and monitoring. Additionally, the compound's stability under various environmental conditions has been evaluated, ensuring its suitability for long-term storage and transportation.

Recent breakthroughs in synthetic chemistry have enabled the development of more efficient methods for the production of Talsupram Hydrochloride. These methods not only enhance the scalability of production but also reduce the environmental impact associated with its synthesis. The use of green chemistry principles in these processes aligns with global efforts to promote sustainable practices in pharmaceutical manufacturing.

In conclusion, Talsupram Hydrochloride (CAS No. 25487-28-9) represents a significant advancement in the field of medicinal chemistry. Its unique properties, coupled with ongoing research into its applications, position it as a promising candidate for addressing unmet medical needs. As further studies continue to unravel its potential, the compound is expected to play a pivotal role in shaping future therapeutic strategies.

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