N-Cyclohexyl-N'-(2-hydroxyethyl)thiourea

Base Information

• Chemical Name: N-Cyclohexyl-N'-(2-hydroxyethyl)thiourea
• CAS No.: 81467-07-4
• Molecular Formula: C9H18N2OS
• Molecular Weight: 202.321
• DSSTox Substance ID: DTXSID20366852
• ChEMBL ID: CHEMBL1486835
• Mol file: 81467-07-4.mol

Synonyms:1-cyclohexyl-3-(2-hydroxyethyl)thiourea;81467-07-4;N-Cyclohexyl-N'-(2-hydroxyethyl)thiourea;Thiourea, N-cyclohexyl-N'-(2-hydroxyethyl)-;SMR000122719;1-Cyclohexyl-3-(2-hydroxy-ethyl)-thiourea;Maybridge1_006090;Oprea1_845920;MLS000523646;SCHEMBL5878686;CHEMBL1486835;HMS558M18;CCG-646;DTXSID20366852;OSSNZOUVMDUFJA-UHFFFAOYSA-N;HMS2363B18;AKOS000511277

Chemical Property of N-Cyclohexyl-N'-(2-hydroxyethyl)thiourea

Chemical Property:

• XLogP3: 1.1
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 202.11398438
• Heavy Atom Count: 13
• Complexity: 158

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(CC1)NC(=S)NCCO

Technology Process of N-Cyclohexyl-N'-(2-hydroxyethyl)thiourea

There total 2 articles about N-Cyclohexyl-N'-(2-hydroxyethyl)thiourea 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-isothiocyanato-ethoxy)dimethyl-silane (455256-33-4) + cyclohexylamine (108-91-8,157973-60-9) → N-cyclohexyl-N'-(2-hydroxyethyl)thiourea (81467-07-4)

Guidance literature:

Reference yield:

cyclohexylamine (108-91-8,157973-60-9) → N-cyclohexyl-N'-(2-hydroxyethyl)thiourea (81467-07-4)

Guidance literature:

Multi-step reaction with 2 steps

1: dicyclohexyl-carbodiimide / dichloromethane / 15 h / -10 - 20 °C / Inert atmosphere

2: tetrahydrofuran / 16 h / Inert atmosphere

With dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane;

DOI:10.1016/j.ejphar.2016.10.009

Reference yield: 97.0%

N-cyclohexyl-N'-(2-hydroxyethyl)thiourea (81467-07-4) → N-cyclohexyl-4,5-dihydro-1,3-thiazol-2-amine (56242-66-1)

Guidance literature:

With hydrogenchloride;

upstream raw materials:

tert-butyl(2-isothiocyanato-ethoxy)dimethyl-silane

cyclohexylamine

Downstream raw materials:

N-cyclohexyl-4,5-dihydro-1,3-thiazol-2-amine

N₃-cyclohexyl-N₁-(2-hydroxyethyl)-N₁-nitrosothiourea

3-cyclohexyl-1-(2-chloroethyl)thiourea

2-hydroxyethyl-N-cyclohexylthionocarbamate