2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanamine hydrochloride

Base Information

• Chemical Name: 2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanamine hydrochloride
• CAS No.: 102441-39-4
• Molecular Formula: C22H20 N2
• Molecular Weight: 312.41
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID90585573
• Mol file: 102441-39-4.mol

Synonyms:102441-39-4;2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanamine hydrochloride;2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethan-1-amine hydrochloride;2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanamine;hydrochloride;2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethan-1-amine;DTXSID90585573;CEA44139;CS-0285736;EN300-05734;2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanaminehydrochloride;2-Phenyl-2-(2-phenyl-1H-indol-3-yl)ethan-1-amine--hydrogen chloride (1/1);1049762-74-4

Chemical Property of 2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanamine hydrochloride

Chemical Property:

• Vapor Pressure: 7.73E-12mmHg at 25°C
• Boiling Point: 542.7°Cat760mmHg
• Flash Point: 315.8°C
• PSA: 41.81000
• Density: g/cm³
• LogP: 6.42780
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 348.1393264
• Heavy Atom Count: 25
• Complexity: 383

Purity/Quality:

2-Phenyl-2-(2-phenyl-1H-indol-3-yl)ethan-1-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=C(C3=CC=CC=C3N2)C(CN)C4=CC=CC=C4.Cl

Technology Process of 2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanamine hydrochloride

There total 2 articles about 2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethanamine 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: 90.0%

rac-3-(2-nitro-1-phenylethyl)-2-phenyl-1H-indole (102704-40-5,889860-85-9) → 2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethan-1-amine (102441-39-4)

Guidance literature:

With sodium tetrahydroborate; nickel(II) chloride hexahydrate; In methanol; at 0 ℃; for 0.5h; Inert atmosphere;

DOI:10.1021/acs.jmedchem.9b00252

Reference yield:

→ 2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethan-1-amine (102441-39-4)

Guidance literature:

With ethanol; nickel; Hydrogenation;

DOI:10.1021/ja01514a048

Reference yield:

2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethan-1-amine (102441-39-4) + methanesulfonyl chloride (124-63-0) → N-(2-phenyl-2-(2-phenyl-1H-indol-3-yl)ethyl)methanesulfonamide

Guidance literature:

With pyridine; dmap; In dichloromethane; at 0 ℃; for 3h; Inert atmosphere;

DOI:10.1021/acs.jmedchem.9b00252

upstream raw materials:

rac-3-(2-nitro-1-phenylethyl)-2-phenyl-1H-indole

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