L3Zwn2hon0

Base Information

Chemical Name:L3Zwn2hon0
CAS No.:176223-33-9
Molecular Formula:C₁₉H₂₆N₂O₅S
Molecular Weight:394.492
Hs Code.:
UNII:L3ZWN2HON0
Nikkaji Number:J732.279H

Synonyms:Ranbaxy-9001;L3ZWN2HON0;RBX9001;RBX-9001;UNII-L3ZWN2HON0;5-((2R)-2-(2-(2-Ethoxyphenoxy)ethylamino)propyl)-2-hydroxy-benzenesulfonamide;Benzenesulfonamide, 5-((2R)-2-((2-(2-ethoxyphenoxy)ethyl)amino)propyl)-2-hydroxy-;176223-33-9;5-[(R)-2-[[2-(2-Ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide

Suppliers and Price of L3Zwn2hon0

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
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Total 0 raw suppliers

Chemical Property of L3Zwn2hon0

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:10
Exact Mass:394.15624311
Heavy Atom Count:27
Complexity:525

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC1=CC=CC=C1OCCNC(C)CC2=CC(=C(C=C2)O)S(=O)(=O)N
Isomeric SMILES:CCOC1=CC=CC=C1OCCN[C@H](C)CC2=CC(=C(C=C2)O)S(=O)(=O)N

Technology Process of L3Zwn2hon0

There total 3 articles about L3Zwn2hon0 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:

: 622853-22-9
R-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide hydrochloride

: 176223-33-9
R-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide

Guidance literature:: R-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide hydrochloride; With 2-(2-ethoxyphenoxy)acetaldehyde; sodium cyanoborohydride; In methanol; at 10 - 20 ℃; for 20h;

With hydrogenchloride; In methanol; for 0.5h; pH=3.0;

With ammonia; In water; at 10 ℃; for 1h; pH=9.0;

Reference yield:

: 103181-55-1
2-(2-ethoxyphenoxy)acetaldehyde

: 622853-26-3
R-5-(2-aminopropyl)-2-hydroxybenzenesulfonamide hydrochloride

: 176223-33-9
R-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide

Guidance literature:: With sodium cyanoborohydride; In methanol; at 20 ℃; for 20h; Product distribution / selectivity;

Reference yield:

: 103181-55-1
2-(2-ethoxyphenoxy)acetaldehyde

: 622853-22-9
R-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide hydrochloride

: 176223-33-9
R-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide

Guidance literature:: 2-(2-ethoxyphenoxy)acetaldehyde; R-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-hydroxybenzenesulfonamide hydrochloride; With sodium cyanoborohydride; In methanol; at 10 - 20 ℃; for 20h;

With hydrogenchloride; In methanol; water; for 0.5h; pH=~ 3.0; Product distribution / selectivity;