(S)-Xamoterol

Base Information

Chemical Name:(S)-Xamoterol
CAS No.:69630-22-4
Molecular Formula:C₁₆H₂₅N₃O₅
Molecular Weight:339.392
Hs Code.:
UNII:ZIB581LRDV
Nikkaji Number:J259.981C
Mol file:69630-22-4.mol

Synonyms:(S)-Xamoterol;69630-22-4;Xamoterol, (S)-;ZIB581LRDV;(S)-N-(2-((2-Hydroxy-3-(4-hydroxyphenoxy)propyl)amino)ethyl)morpholine-4-carboxamide;4-Morpholinecarboxamide, N-(2-(((2S)-2-hydroxy-3-(4-hydroxyphenoxy)propyl)amino)ethyl)-;4-Morpholinecarboxamide, N-(2-((2-hydroxy-3-(4-hydroxyphenoxy)propyl)amino)ethyl)-, (S)-;UNII-ZIB581LRDV;SCHEMBL11533496;N-[2-[[(2S)-2-Hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethyl]morpholine-4-carboxamide;NS00068564

Suppliers and Price of (S)-Xamoterol

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of (S)-Xamoterol

Chemical Property:

PSA：103.29000
LogP:0.48300
XLogP3:-0.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:8
Exact Mass:339.17942091
Heavy Atom Count:24
Complexity:358

Purity/Quality:: 99.3% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1COCCN1C(=O)NCCNCC(COC2=CC=C(C=C2)O)O
Isomeric SMILES:C1COCCN1C(=O)NCCNC[C@@H](COC2=CC=C(C=C2)O)O

Technology Process of (S)-Xamoterol

There total 10 articles about (S)-Xamoterol 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: 91.7%

: 122715-70-2,69630-21-3
(S)-N-(2-(3-(4-(benzyloxy)phenoxy)-2-hydroxypropylamino)ethyl)morpholine-4-carboxamide

: 1229516-19-1,69630-22-4
(S)-Xamoterol

Guidance literature:: With 10 wt% Pd(OH)2 on carbon; acetic acid; In ethanol; under 2844.39 Torr;

Reference yield:

: 122715-70-2,69630-21-3
(S)-N-(2-(3-(4-(benzyloxy)phenoxy)-2-hydroxypropylamino)ethyl)morpholine-4-carboxamide

: 110-17-8,26099-09-2
(2E)-but-2-enedioic acid

: 1229516-19-1,69630-22-4
(S)-Xamoterol

Guidance literature:: With acetic acid; palladium; In ethanol;

Reference yield:

: 69630-06-4
phenyl N-<2--2-hydroxypropyl>amino>ethyl>carbamate

: 81801-12-9,1229516-19-1,69630-22-4
xamoterol

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 18 h / 100 °C

2: H₂, AcOH / 30percent Pd/C / 1.5 h

With hydrogen; acetic acid; palladium on activated charcoal; In toluene;
DOI:10.1021/jm00135a015