Phenyl N-(4-methylphenyl)carbamate

Base Information

• Chemical Name: Phenyl N-(4-methylphenyl)carbamate
• CAS No.: 33275-26-2
• Molecular Formula: C14H13NO2
• Molecular Weight: 227.263
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID40401496
• Nikkaji Number: J1.656.189D
• Wikidata: Q82204635

Synonyms:33275-26-2;Phenyl p-tolylcarbamate;Carbamic acid, (4-methylphenyl)-, phenyl ester;Phenyl N-(4-methylphenyl)carbamate;Phenylp-tolylcarbamate;phenyl 4-methylphenylcarbamate;SCHEMBL6037499;phenyl-(4-methylphenyl)carbamate;DTXSID40401496;AKOS008917353;CS-0247483;EN300-366861;Z28135008

Chemical Property of Phenyl N-(4-methylphenyl)carbamate

Chemical Property:

• PSA: 38.33000
• LogP: 3.67890
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 227.094628657
• Heavy Atom Count: 17
• Complexity: 241

Purity/Quality:

99% ^*data from raw suppliers

PHENYL N-(P-TOLYL)CARBAMATE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)NC(=O)OC2=CC=CC=C2

Technology Process of Phenyl N-(4-methylphenyl)carbamate

There total 8 articles about Phenyl N-(4-methylphenyl)carbamate 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: 94.0%

p-toluidine (106-49-0,12221-03-3) + phenyl chloroformate (1885-14-9) → N-(4-methylphenyl)-O-phenyl carbamate (33275-26-2)

Guidance literature:

With pyridine; In dichloromethane; for 3h; Ambient temperature;

DOI:10.1021/jo981816+

Reference yield: 92.0%

phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate (1202680-24-7) + p-toluidine (106-49-0,12221-03-3) → N-(4-methylphenyl)-O-phenyl carbamate (33275-26-2)

Guidance literature:

In tetrahydrofuran; at 20 ℃; for 0.166667h;

DOI:10.1055/s-0029-1217997

Reference yield: 89.0%

bis(phenyl) carbonate (102-09-0) + 1,3-di-p-tolylurea (621-00-1) → N-(4-methylphenyl)-O-phenyl carbamate (33275-26-2)

Guidance literature:

With silica gel; at 150 ℃; for 8h;

DOI:10.1039/b107947f

upstream raw materials:

bis(phenyl) carbonate

p-toluidine

phenyl chloroformate

1,3-di-p-tolylurea

Downstream raw materials:

N-(4-methylphenyl)-3-endo-(phenylsulfonyl)-8-azabicyclo[3.2.1]octane-8-carboxamide

N-4-Methylphenyl-N',N'-pentamethylenharnstoff

1-(4-methylphenyl)-3-cyclohexylurea

N-butyl-N’-(4-methylphenyl)urea

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
  FOB CIF CFR EXW
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 33275-26-2 Carbamic acid, (4-methylphenyl)-, phenyl ester

Send

Send

Metric Ton KG G Pound L ML

Send

Send