Glemanserin, (R)-

Base Information Edit

Chemical Name:Glemanserin, (R)-
CAS No.:132553-87-8
Molecular Formula:C₂₀H₂₅NO
Molecular Weight:295.425
Hs Code.:
UNII:1PO4YCI5ZE
Nikkaji Number:J549.471K
ChEMBL ID:CHEMBL1435444
Mol file:132553-87-8.mol

Synonyms:Glemanserin, (R)-;1PO4YCI5ZE;UNII-1PO4YCI5ZE;132553-87-8;4-Piperidinemethanol, alpha-phenyl-1-(2-phenylethyl)-, (R)-;(R)-(+)-alpha-Phenyl-(1-(2-phenylethyl))-4-piperidinemethanol;Tocris-0870;CHEMBL1435444;NCGC00024833-01;(alphaR)-alpha-Phenyl-1-(2-phenylethyl)-4-piperidinemethanol;(R)-(+)-.ALPHA.-PHENYL-(1-(2-PHENYLETHYL))-4-PIPERIDINEMETHANOL;4-PIPERIDINEMETHANOL, .ALPHA.-PHENYL-1-(2-PHENYLETHYL)-, (R)-

Suppliers and Price of Glemanserin, (R)-

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Glemanserin, (R)- Edit

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:295.193614421
Heavy Atom Count:22
Complexity:299

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN(CCC1C(C2=CC=CC=C2)O)CCC3=CC=CC=C3
Isomeric SMILES:C1CN(CCC1[C@H](C2=CC=CC=C2)O)CCC3=CC=CC=C3

Technology Process of Glemanserin, (R)-

There total 6 articles about Glemanserin, (R)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 68.0%

: 1-phenylethyl-4-benzoyl-3H-pyridine-2,6-dione

: 107703-78-6,132553-86-7,132553-87-8,132553-88-9
glemanserin

Guidance literature:: 1-phenylethyl-4-benzoyl-3H-pyridine-2,6-dione; With hydrogen; palladium on activated charcoal; In tetrahydrofuran; at 20 ℃; for 3h;

With lithium aluminium tetrahydride; aluminium trichloride; In tetrahydrofuran; for 2h; Heating;