Deterenol hydrochloride

Base Information

• Chemical Name: Deterenol hydrochloride
• CAS No.: 23239-36-3
• Molecular Formula: C11H17 N O2 . Cl H
• Molecular Weight: 231.722
• Hs Code.: 2922509090
• UNII: RCH64O2H56
• DSSTox Substance ID: DTXSID00945922
• Wikidata: Q27288055
• NCI Thesaurus Code: C169888
• ChEMBL ID: CHEMBL2106513
• Mol file: 23239-36-3.mol

Synonyms:1-(4-hydroxyphenyl)-2-isopropylaminoethanol;AL 842;deterenol;deterenol hydrochloride, (+-)-isomer;deterenol oxalate (2:1), (+-)-isomer;deterenol sulfate (1:1);deterenol, (+-)-isomer;N-isopropylnorsynephrine;N-isopropyloctopamine;PI 39;PI-39

Chemical Property of Deterenol hydrochloride

Chemical Property:

• Vapor Pressure: 1.11E-05mmHg at 25°C
• Melting Point: 155-157 °C
• Boiling Point: 355.9°Cat760mmHg
• Flash Point: 143°C
• PSA: 52.49000
• Density: g/cm³
• LogP: 2.61650
• Storage Temp.: Hygroscopic, -20°C Freezer, Under Inert Atmosphere
• Solubility.: DMSO (Slightly), Water (Slightly)
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 231.1026065
• Heavy Atom Count: 15
• Complexity: 153

Purity/Quality:

98%Min ^*data from raw suppliers

DeterenolHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)NCC(C1=CC=C(C=C1)O)O.Cl
• Uses: Deterenol Hydrochloride is an effective, nonmydriatic and nonmiotic hypotensive agent with intraocular pressure (IOP) effects similar to epinephrine bitartrate in rhesus monkeys when administered at approx. twice the concentration of epinephrine used clinically.

Technology Process of Deterenol hydrochloride

There total 1 articles about Deterenol hydrochloride 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: 91.0%

1-(4-hydroxy-phenyl)-2-isopropylamino-ethanone; hydrochloride (69716-74-1) → Paraproterenol hydrochloride (23239-36-3)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃; for 24h; under 760.051 Torr;

upstream raw materials:

1-(4-hydroxy-phenyl)-2-isopropylamino-ethanone; hydrochloride