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1-(4-methylsulfanylphenyl)propylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1204749-80-3

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1204749-80-3 Usage

Type of compound

Organic chemical compound

Structure

Contains a phenyl ring
Methylthio substituent at the 4-position of the phenyl ring
Propylamine group attached to the phenyl ring

Properties

Amine compound
Structural similarity to certain neurotransmitters

Potential applications

Pharmaceutical industry (building block for synthesis of biologically active compounds)
Research tool (study of neural pathways and dopamine receptors)
Organic synthesis and medicinal chemistry (development of new drugs and pharmaceutical agents)

Versatility

Wide range of potential applications in scientific and industrial fields

Check Digit Verification of cas no

The CAS Registry Mumber 1204749-80-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,7,4 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1204749-80:
(9*1)+(8*2)+(7*0)+(6*4)+(5*7)+(4*4)+(3*9)+(2*8)+(1*0)=143
143 % 10 = 3
So 1204749-80-3 is a valid CAS Registry Number.

1204749-80-3Downstream Products

1204749-80-3Relevant academic research and scientific papers

Synthesis and serotonin transporter activity of sulphur-substituted α-alkyl phenethylamines as a new class of anticancer agents

Cloonan, Suzanne M.,Keating, John J.,Butler, Stephen G.,Knox, Andrew J.S.,Jorgensen, Anne M.,Peters, Guenther H.,Rai, Dilip,Corrigan, Desmond,Lloyd, David G.,Williams, D. Clive,Meegan, Mary J.

experimental part, p. 4862 - 4888 (2010/01/16)

The discovery that some serotonin reuptake transporter (SERT) ligands have the potential to act as pro-apoptotic agents in the treatment of cancer adds greatly to their diverse pharmacological application. 4-Methylthioamphetamine (MTA) is a selective ligand for SERT over other monoamine transporters. In this study, a novel library of structurally diverse 4-MTA analogues were synthesised with or without N-alkyl and/or C-α methyl or ethyl groups so that their potential SERT-dependent antiproliferative activity could be assessed. Many of the compounds displayed SERT-binding activity as well as cytotoxic activity. While there was no direct correlation between these two effects, a number of derivatives displayed anti-tumour effects in lymphoma, leukaemia and breast cancer cell lines, showing further potential to be developed as possible chemotherapeutic agents.

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