Carbamic acid, dibutyl-, butyl ester

Base Information

• Chemical Name: Carbamic acid, dibutyl-, butyl ester
• CAS No.: 27000-73-3
• Molecular Formula: C13H27NO2
• Molecular Weight: 229.363
• DSSTox Substance ID: DTXSID20472361
• Nikkaji Number: J532.484J
• Wikidata: Q82301256

Synonyms:Carbamic acid, dibutyl-, butyl ester;SCHEMBL65775;27000-73-3;DTXSID20472361

Chemical Property of Carbamic acid, dibutyl-, butyl ester

Chemical Property:

• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 10
• Exact Mass: 229.204179104
• Heavy Atom Count: 16
• Complexity: 163

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCN(CCCC)C(=O)OCCCC

Technology Process of Carbamic acid, dibutyl-, butyl ester

There total 6 articles about Carbamic acid, dibutyl-, butyl ester 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: 95.6%

butyl phenyl carbonate (4824-76-4) + dibutylamine (111-92-2) → butyl-N,N-dibutylurethane (27000-73-3) + phenol (108-95-2,27073-41-2)

Guidance literature:

In N,N-dimethyl-formamide; at 100 - 105 ℃; for 5h;

Reference yield:

4-nitrophenyl butyl carbonate (67036-13-9) + dibutylamine (111-92-2) → 4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) + butyl-N,N-dibutylurethane (27000-73-3)

Guidance literature:

In N,N-dimethyl-formamide; at 100 - 105 ℃; for 5h; Yield given;

Reference yield:

1-bromo-butane (109-65-9) + carbon dioxide (124-38-9,18923-20-1) + dibutylamine (111-92-2) → tributyl-amine (102-82-9) + butyl-N,N-dibutylurethane (27000-73-3)

Guidance literature:

With caesium carbonate; at 20 ℃; for 24h; under 760.051 Torr; chemoselective reaction;

DOI:10.1080/00397911.2010.517890

upstream raw materials:

butyl phenyl carbonate

dibutylamine

Kohlensaeure-butyl-m-tolyl-ester

4-nitrophenyl butyl carbonate

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