2-(4-Chlorophenoxy)ethanimidamide hydrochloride

Base Information

• Chemical Name: 2-(4-Chlorophenoxy)ethanimidamide hydrochloride
• CAS No.: 59104-19-7
• Molecular Formula: C₈H₉ClN₂O*ClH
• Molecular Weight: 221.086
• Hs Code.: 2925290090
• European Community (EC) Number: 800-945-6
• DSSTox Substance ID: DTXSID50540582
• Mol file: 59104-19-7.mol

Synonyms:59104-19-7;2-(4-Chlorophenoxy)ethanimidamide hydrochloride;2-(4-Chlorophenoxy)acetamidine hydrochloride;2-(4-Chlorophenoxy)acetimidamide hydrochloride;2-(4-chloro-phenoxy)-acetamidine hydrochloride;2-(4-chlorophenoxy)ethanimidamide;hydrochloride;MFCD00464961;2-(4-chlorophenoxy)ethanimidamide,hydrochloride;SCHEMBL5480598;NIOSH/AD0619000;Su-332;DTXSID50540582;2-(4-Chloro-phenoxy)-acetamidine hcl;AKOS024458760;2,3,4,5,6-Pentafluorobenzyl Brimide;SB37829;TS-03159;2-(4-Chlorophenoxy)acetimidamidehydrochloride;AD06190000;CS-0317504;A917855;Acetamidine, 2-(p-chlorophenoxy)-, hydrochloride;(4-Chlorophenoxy)ethanimidamide--hydrogen chloride (1/1)

Chemical Property of 2-(4-Chlorophenoxy)ethanimidamide hydrochloride

Chemical Property:

• Vapor Pressure: 0.000774mmHg at 25°C
• Melting Point: 185-187 °C
• Boiling Point: 306.4 °C at 760 mmHg
• Flash Point: 139.1 °C
• PSA: 59.10000
• LogP: 3.25680
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 220.0170183
• Heavy Atom Count: 13
• Complexity: 155

Purity/Quality:

98%Min ^*data from raw suppliers

2-(4-Chlorophenoxy)acetamidine hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1OCC(=N)N)Cl.Cl

Technology Process of 2-(4-Chlorophenoxy)ethanimidamide hydrochloride

There total 2 articles about 2-(4-Chlorophenoxy)ethanimidamide 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:

(4-chlorophenoxy)acetonitrile (3598-13-8) → 2-(4-chloro-phenoxy)-acetamidine; hydrochloride (59104-19-7)

Guidance literature:

Multi-step reaction with 2 steps

1: HCl

2: NH₃ / ethanol

With hydrogenchloride; ammonia; In ethanol;

DOI:10.1016/S0040-4039(00)98575-7

Reference yield:

Ethyl 2-(4-chlorophenoxy)acetimidate hydrochloride (3598-08-1) → 2-(4-chloro-phenoxy)-acetamidine; hydrochloride (59104-19-7)

Guidance literature:

With ammonia; In ethanol;

DOI:10.1016/S0040-4039(00)98575-7

Reference yield:

2-(4-chloro-phenoxy)-acetamidine; hydrochloride (59104-19-7) → 3-Chloro-3-(4-chloro-phenoxymethyl)-3H-diazirine

Guidance literature:

With sodium hypochlorite; In tetrachloromethane; dimethyl sulfoxide;

DOI:10.1016/S0040-4039(00)98575-7

upstream raw materials:

(4-chlorophenoxy)acetonitrile

Ethyl 2-(4-chlorophenoxy)acetimidate hydrochloride

Downstream raw materials:

1-Chloro-4-((E)-2-chloro-vinyloxy)-benzene

Refernces