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(S)-1-(3,4-Dichloro-phenyl)-propylamine, with the molecular formula C9H12Cl2N, is an amine compound characterized by a propyl group and two chlorine atoms attached to a phenyl ring. (S)-1-(3,4-Dichloro-phenyl)-propylamine is recognized as a selective dopamine reuptake inhibitor, which can prevent the reuptake of dopamine in the brain, thereby increasing dopamine levels in the synaptic cleft. This increase in dopamine may influence mood, motivation, and other brain functions. Additionally, (S)-1-(3,4-Dichloro-phenyl)-propylamine may have other physiological effects due to its interaction with dopamine receptors.

847448-45-7

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847448-45-7 Usage

Uses

Used in Neuroscience Research:
(S)-1-(3,4-Dichloro-phenyl)-propylamine is used as a research tool for studying the role of dopamine in the brain. Its ability to inhibit dopamine reuptake makes it a valuable compound for understanding the mechanisms behind mood regulation, motivation, and other cognitive functions related to dopamine.
Used in Pharmacology:
In the field of pharmacology, (S)-1-(3,4-Dichloro-phenyl)-propylamine is used as a starting point for developing new treatments for dopamine-related disorders. Its selective dopamine reuptake inhibition property can be harnessed to create medications that target conditions such as Parkinson's disease, attention deficit hyperactivity disorder (ADHD), and other mood disorders where dopamine dysregulation is implicated.
Used in Drug Development:
(S)-1-(3,4-Dichloro-phenyl)-propylamine serves as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs that can modulate dopamine levels in the brain, potentially leading to more effective treatments for a range of neurological and psychiatric conditions.
Used in Chemical Synthesis:
Beyond its direct applications in neuroscience and pharmacology, (S)-1-(3,4-Dichloro-phenyl)-propylamine can also be utilized in the broader field of chemical synthesis. Its unique structure and functional groups make it a versatile building block for creating a variety of other compounds with different applications in various industries, such as materials science, agrochemicals, and more.

Check Digit Verification of cas no

The CAS Registry Mumber 847448-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,4,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 847448-45:
(8*8)+(7*4)+(6*7)+(5*4)+(4*4)+(3*8)+(2*4)+(1*5)=207
207 % 10 = 7
So 847448-45-7 is a valid CAS Registry Number.

847448-45-7Upstream product

847448-45-7Relevant academic research and scientific papers

MERCAPTOIMIDAZOLES AS CCR2 RECEPTOR ANTAGONISTS

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Page/Page column 35, (2010/10/19)

The present invention relates to a compound of formula (I), aN-oxide, a pharmaceutically acceptable addition salt, a quaternary amine and a stereochemically isomeric form thereof, wherein R1 represents hydrogen, C1-6alkyl, C3-7

MERCAPTOIMIDAZOLES AS CCR2 RECEPTOR ANTAGONISTS

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Page/Page column 46, (2008/06/13)

The present invention relates to a compound of formula (I) a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine, a polymorphic form or a stereochemically isomeric form thereof, wherein R1 represents hydrogen, C1-6alkyl, C3-7cycloalky

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