2-(5-Bromothiophen-2-yl)ethanamine hydrobromide

Base Information

• Chemical Name: 2-(5-Bromothiophen-2-yl)ethanamine hydrobromide
• CAS No.: 381666-13-3
• Molecular Formula: BrH*C₆H₈BrNS
• Molecular Weight: 287.018
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID10585878
• Mol file: 381666-13-3.mol

Synonyms:2-(5-Bromothiophen-2-yl)ethanamine hydrobromide;381666-13-3;2-(5-bromothiophen-2-yl)ethan-1-amine hydrobromide;2-(5-bromothiophen-2-yl)ethanamine;hydrobromide;C6H9Br2NS;DTXSID10585878;AKOS016007420;EN300-12509;2-(5-Bromothiophen-2-yl)ethanaminehydrobromide;F8888-5438;2-(5-Bromothiophen-2-yl)ethan-1-amine--hydrogen bromide (1/1)

Chemical Property of 2-(5-Bromothiophen-2-yl)ethanamine hydrobromide

Chemical Property:

• PSA: 54.26000
• LogP: 3.67020
• Storage Temp.: Sealed in dry,Room Temperature
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 286.88020
• Heavy Atom Count: 10
• Complexity: 89.1

Purity/Quality:

99%min ^*data from raw suppliers

2-(5-Bromothiophen-2-yl)ethanamine hydrobromide 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=C(SC(=C1)Br)CCN.Br

Technology Process of 2-(5-Bromothiophen-2-yl)ethanamine hydrobromide

There total 2 articles about 2-(5-Bromothiophen-2-yl)ethanamine 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:

tert-butyl (2-(thiophen-2-yl)ethyl)carbamate (381666-12-2) → 5-bromothiophenethylamine hydrobromide (381666-13-3)

Guidance literature:

With bromine; In acetic acid; at 0 - 20 ℃;

DOI:10.1016/S0040-4039(01)01290-4

Reference yield:

[2-(2-thyenyl)ethyl]amine (30433-91-1) → 5-bromothiophenethylamine hydrobromide (381666-13-3)

Guidance literature:

Multi-step reaction with 2 steps

1: CHCl₃ / 6 h / Heating

2: Br₂ / acetic acid / 0 - 20 °C

With bromine; In chloroform; acetic acid;

DOI:10.1016/S0040-4039(01)01290-4

upstream raw materials:

tert-butyl (2-(thiophen-2-yl)ethyl)carbamate

[2-(2-thyenyl)ethyl]amine

Refernces