Urea, N-(1-methylethyl)-N'-(phenylmethyl)-

Base Information

• Chemical Name: Urea, N-(1-methylethyl)-N'-(phenylmethyl)-
• CAS No.: 71819-34-6
• Molecular Formula: C11H16N2O
• Molecular Weight: 192.261
• European Community (EC) Number: 666-123-2
• DSSTox Substance ID: DTXSID90397491
• Nikkaji Number: J869.413C
• Wikidata: Q82198890

Synonyms:Urea, N-(1-methylethyl)-N'-(phenylmethyl)-;71819-34-6;1-benzyl-3-propan-2-ylurea;1-Isopropyl-3-benzylurea;N-benzyl-N'-isopropylurea;SCHEMBL12252067;DTXSID90397491;AKOS016495640

Chemical Property of Urea, N-(1-methylethyl)-N'-(phenylmethyl)-

Chemical Property:

• XLogP3: 1.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 192.126263138
• Heavy Atom Count: 14
• Complexity: 174

Purity/Quality:

99.0% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)NC(=O)NCC1=CC=CC=C1

Technology Process of Urea, N-(1-methylethyl)-N'-(phenylmethyl)-

There total 10 articles about Urea, N-(1-methylethyl)-N'-(phenylmethyl)- 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%

N-benzyl-N'-isopropylthiourea (70498-23-6) → N-benzyl-N’-isopropylurea (71819-34-6)

Guidance literature:

With potassium dichloroiodate; In water; acetonitrile; for 1.5h; Time; Temperature; Reflux;

DOI:10.1016/j.tetlet.2012.12.045

Reference yield: 84.0%

Benzyl isothiocyanate (622-78-6) + isopropylamine (75-31-0) → N-benzyl-N’-isopropylurea (71819-34-6)

Guidance literature:

With 3,3-dimethyldioxirane; In acetone; for 0.25h; Ambient temperature;

Reference yield: 74.0%

Benzeneacetamide (103-81-1) + isopropylamine (75-31-0) → N-benzyl-N’-isopropylurea (71819-34-6)

Guidance literature:

With iodosylbenzene; In dichloromethane; at 20 ℃; for 2h;

DOI:10.1002/ejoc.201101784

upstream raw materials:

chloromethyl N-benzyl carbamate

isopropylamine

benzylamine

Isopropyl isocyanate

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