2-Amino-1-(furan-2-YL)ethanone hydrochloride

Base Information

• Chemical Name: 2-Amino-1-(furan-2-YL)ethanone hydrochloride
• CAS No.: 88352-86-7
• Molecular Formula: C6H7NO2.ClH
• Molecular Weight: 161.588
• European Community (EC) Number: 863-859-8
• DSSTox Substance ID: DTXSID10530040
• Mol file: 88352-86-7.mol

Synonyms:88352-86-7;2-AMINO-1-(FURAN-2-YL)ETHANONE HYDROCHLORIDE;2-amino-1-(furan-2-yl)ethan-1-one hydrochloride;2-amino-1-(furan-2-yl)ethanone;hydrochloride;SCHEMBL4971503;DTXSID10530040;RKEARERKYHKVQD-UHFFFAOYSA-N;AMY15091;2-Amino-1-(2-Furyl)ethanone HCl;MFCD18917270;2-amino-1-(furan-2-yl)ethanone HCl;AKOS026742759;2-furyl aminomethyl ketone hydrochloride;(2-furylcarbonyl)methylamine hydrochloride;SY190554;2-Amino-1-(2-furyl)ethanone Hydrochloride;CS-0261145;EN300-77341;A846951;2-AMINO-1-(FURAN-2-YL)ETHANONEHYDROCHLORIDE;Z1193968923;2-Amino-1-(furan-2-yl)ethan-1-one--hydrogen chloride (1/1)

Chemical Property of 2-Amino-1-(furan-2-YL)ethanone hydrochloride

Chemical Property:

• Melting Point: 222-223 °C (decomp)
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 161.0243562
• Heavy Atom Count: 10
• Complexity: 114

Purity/Quality:

97% ^*data from raw suppliers

2-amino-1-(furan-2-yl)ethan-1-onehydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=COC(=C1)C(=O)CN.Cl

Technology Process of 2-Amino-1-(furan-2-YL)ethanone hydrochloride

There total 4 articles about 2-Amino-1-(furan-2-YL)ethanone 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: 98.0%

methyl 2-amino-3-(furan-2-yl)-3-oxopropionate hydrochoride (93102-94-4) → (furan-2-ylcarbonyl)methylamine hydrochloride (88352-86-7)

Guidance literature:

With hydrogenchloride;

DOI:10.1248/cpb.32.2536

Reference yield: 82.0%

→ (furan-2-ylcarbonyl)methylamine hydrochloride (88352-86-7)

Guidance literature:

Reference yield:

5-Furan-2-yl-oxazole-4-carboxylic acid methyl ester (89205-03-8) → (furan-2-ylcarbonyl)methylamine hydrochloride (88352-86-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 89 percent / HCl

2: 98 percent / HCl

With hydrogenchloride;

DOI:10.1248/cpb.32.2536

upstream raw materials:

methyl 2-amino-3-(furan-2-yl)-3-oxopropionate hydrochoride

5-Furan-2-yl-oxazole-4-carboxylic acid methyl ester

Downstream raw materials:

2-amino-1-[2]furyl-ethanone-(4-nitro-phenylhydrazone); hydrochloride

N-(4-fluorobenzoyl)-(furan-2-ylcarbonyl)methylamine

N-(2-Furan-2-yl-2-oxo-ethyl)-3-trifluoromethyl-benzamide

N-benzoyl-(furan-2-ylcarbonyl)methylamine