Benzeneethanamine, hydrobromide

Base Information

• Chemical Name: Benzeneethanamine, hydrobromide
• CAS No.: 53916-94-2
• Molecular Formula: C8H11N.BrH
• Molecular Weight: 202.094
• Mol file: 53916-94-2.mol

Synonyms:phenethylammonium bromide;phenylethylamine hydrobromide;Hydrobromid;Phenaethylamin;phenethylamine;phenylethylammonium bromide;hydrobromide;

Chemical Property of Benzeneethanamine, hydrobromide

Chemical Property:

• Melting Point: 259°C(lit.)
• PSA: 26.02000
• LogP: 2.84620

Purity/Quality:

98%,99%, ^*data from raw suppliers

2-PhenylethylamineHydrobromide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Organohalide based perovskites have emerged as an important class of material for solar cell applications. Our perovskites precursors are useful for synthesizing mixed cation or anion perovskites needed for the optimization of the band gap, carrier diffusion length and power conversion efficiency of perovskites based solar cells.

Technology Process of Benzeneethanamine, hydrobromide

There total 2 articles about Benzeneethanamine, hydrobromide 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: 93.0%

1-phenyl-2-bromoethane (103-63-9) → β-phenethylammonium bromide (53916-94-2)

Guidance literature:

With ammonium hydroxide; In methanol; at 160 ℃; for 0.166667h; under 18100.7 Torr; Temperature; chemoselective reaction; Flow reactor;

DOI:10.1021/acs.joc.8b02387

Reference yield:

phenethylamine (64-04-0) → β-phenethylammonium bromide (53916-94-2)

Guidance literature:

With hydrogen bromide; In ethanol; for 3h; Cooling with ice;

DOI:10.1039/d0dt00514b

Reference yield: 83.0%

β-phenethylammonium bromide (53916-94-2) + Ethyl 2-bromopropionate (535-11-5,41978-69-2) → 2-[1-(2-phenylethyl)amino]propionic acid ethyl ester

Guidance literature:

With triethylamine; In N,N-dimethyl-formamide; at 20 - 25 ℃; for 10h; chemoselective reaction; Molecular sieve;

DOI:10.1039/c4ra01915f

upstream raw materials:

1-phenyl-2-bromoethane

phenethylamine

Downstream raw materials:

2-phenylethylammonium lead bromide