(2s)-1-(9h-Carbazol-4-Yloxy)-3-(Isopropylamino)propan-2-Ol

Base Information

• Chemical Name: (2s)-1-(9h-Carbazol-4-Yloxy)-3-(Isopropylamino)propan-2-Ol
• CAS No.: 78859-33-3
• Molecular Formula: C18H22 N2 O2
• Molecular Weight: 298.38
• European Community (EC) Number: 890-276-6
• UNII: 6Q9080LN3O
• Metabolomics Workbench ID: 150715
• Nikkaji Number: J1.472.893G
• Wikidata: Q27096765
• Mol file: 78859-33-3.mol

Synonyms:(-)-carazolol;(s)-carazolol;78859-33-3;Carazolol, (S)-;(2s)-1-(9h-Carbazol-4-Yloxy)-3-(Isopropylamino)propan-2-Ol;UNII-6Q9080LN3O;6Q9080LN3O;(2S)-1-(9H-carbazol-4-yloxy)-3-(propan-2-ylamino)propan-2-ol;2-Propanol, 1-(9H-carbazol-4-yloxy)-3-((1-methylethyl)amino)-, (2S)-;CAU;(S)-Carazolol Hydrochloride;SCHEMBL77903;DB07543;EN300-26486077;Q27096765;(S)-1-(Carbazol-4-yloxy)-3-(isopropylamino)-2-propanol;(S)-1-(9H-carbazol-4-yloxy)-3-(isopropylamino)propan-2-ol;(2S)-1-(9H-carbazol-4-yloxy)-3-[(propan-2-yl)amino]propan-2-ol;(2S)-1-(9H-carbazol-4-yloxy)-3-[(1-methylethyl)amino]propan-2-ol

Chemical Property of (2s)-1-(9h-Carbazol-4-Yloxy)-3-(Isopropylamino)propan-2-Ol

Chemical Property:

• PSA: 57.28000
• LogP: 3.44970
• XLogP3: 3.6
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 298.168127949
• Heavy Atom Count: 22
• Complexity: 350

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)NCC(COC1=CC=CC2=C1C3=CC=CC=C3N2)O
• Isomeric SMILES: CC(C)NC[C@@H](COC1=CC=CC2=C1C3=CC=CC=C3N2)O
• Uses: (S)-Carazolol Hydrochloride is a β-adrenoreceptor antagonist.

Technology Process of (2s)-1-(9h-Carbazol-4-Yloxy)-3-(Isopropylamino)propan-2-Ol

There total 1 articles about (2s)-1-(9h-Carbazol-4-Yloxy)-3-(Isopropylamino)propan-2-Ol 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:

carazolol (57775-29-8) → NSC 305336 (78859-34-4) + (S)-Carazolol (78859-33-3)

Guidance literature:

With AmyCoat (150x46 mm, 3 μm size silica particle); In ethanol; n-heptane; diethylamine; at 27 ℃; Resolution of racemate;

DOI:10.1002/chir.20697

upstream raw materials:

carazolol

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