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131986-45-3

  • Product Name:Xanomeline
  • Molecular Formula:C14H23N3OS
  • Molecular Weight:281.422
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Product Details

Purity:99%

Quality Factory Hot Selling Xanomeline 131986-45-3 with Fast Shipping

  • Molecular Formula:C14H23N3OS
  • Molecular Weight:281.422
  • Vapor Pressure:1.64E-06mmHg at 25°C 
  • Refractive Index:1.537 
  • Boiling Point:397 °C at 760 mmHg 
  • PKA:7.34±0.40(Predicted) 
  • Flash Point:193.9 °C 
  • PSA：66.49000 
  • Density:1.101 g/cm3 
  • LogP:3.15400 

5-(4-HEXYLOXY-[1,2,5]THIADIAZOL-3-YL)-1-METHYL-1,2,3,6-TETRAHYDRO-PYRIDINE(Cas 131986-45-3) Usage

InChI:InChI=1/C14H23N3OS/c1-3-4-5-6-10-18-14-13(15-19-16-14)12-8-7-9-17(2)11-12/h8H,3-7,9-11H2,1-2H3

131986-45-3 Relevant articles

Tacrine-xanomeline and tacrine-iperoxo hybrid ligands: Synthesis and biological evaluation at acetylcholinesterase and M1 muscarinic acetylcholine receptors

Cirillo, Davide,Dallanoce, Clelia,De Amici, Marco,Holzgrabe, Ulrike,Maspero, Marco,Messerer, Regina,Sotriffer, Christoph,Volpato, Daniela,Yuan Chen, Natalia

, (2020/02/11)

We synthesized a set of new hybrid deriv...

Towards the development of new subtype-specific muscarinic receptor radiopharmaceuticals - Radiosynthesis and ex vivo biodistribution of [ 18F]3-(4-(2-(2-(2-fluoroethoxy)ethoxy)ethylthio)-1,2, 5-thiadiazol-3-yl)-1-methyl-1,2,5,6-tetrahydropyrid

Van Oosten, Erik M.,Wilson, Alan A.,Mamo, David C.,Pollock, Bruce G.,Mulsant, Benoit H.,Houle, Sylvain,Vasdev, Neil

experimental part, p. 1222 - 1232 (2011/02/24)

Muscarinic receptors have been implicate...

Synthesis and evaluation of xanomeline analogs-Probing the wash-resistant phenomenon at the M1 muscarinic acetylcholine receptor

Kane, Brian E.,Grant, Marianne K.O.,El-Fakahany, Esam E.,Ferguson, David M.

, p. 1376 - 1392 (2008/09/18)

A series of xanomeline analogs were synt...

Combination therapy for treatment of psychoses

-

, (2008/06/13)

The invention provides combination thera...

131986-45-3 Process route

3-(3-Pentyloxy-1,2,5-thiadiazol-4-yl)-1-methylpyridinium iodide
131988-16-4

3-(3-Pentyloxy-1,2,5-thiadiazol-4-yl)-1-methylpyridinium iodide

xanomeline
131986-45-3

xanomeline

Conditions
Conditions Yield
With methanol; sodium tetrahydroborate; at 20 ℃;
75%
3-(4-hexyloxy-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodide
131988-19-7

3-(4-hexyloxy-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodide

xanomeline
131986-45-3

xanomeline

Conditions
Conditions Yield
With sodium tetrahydroborate; In ethanol; at -10 ℃; for 1h;
With sodium tetrahydroborate; In ethanol;
With sodium tetrahydroborate; In ethanol; for 3h; Heating;

131986-45-3 Upstream products

  • 131988-19-7
    131988-19-7

    3-(4-hexyloxy-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodide

  • 131986-59-9
    131986-59-9

    3-(3-Chloro-1,2,5-thiadiazol-4-yl)-1,2,5,6-tetrahydro-1-methylpyridine

  • 111-27-3
    111-27-3

    hexan-1-ol

  • 500-22-1
    500-22-1

    3-pyridinecarboxaldehyde

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