P-Methyoxyphenol carbanilate

Base Information

• Chemical Name: P-Methyoxyphenol carbanilate
• CAS No.: 19219-48-8
• Molecular Formula: C14H13NO3
• Molecular Weight: 243.262
• DSSTox Substance ID: DTXSID30172789
• Nikkaji Number: J689.475E
• Wikidata: Q83042872
• ChEMBL ID: CHEMBL1366454
• Mol file: 19219-48-8.mol

Synonyms:P-METHYOXYPHENOL CARBANILATE;4-methoxyphenyl phenylcarbamate;19219-48-8;SMR000137180;Oprea1_540815;MLS000532241;CHEMBL1366454;SCHEMBL22204354;DTXSID30172789;HMS1578P13;HMS2479F17;STL324850;AKOS003311340;NCGC00245727-01;Phenylcarbamic acid 4-methoxyphenyl ester;AB00075551-01;SR-01000198983;SR-01000198983-1

Chemical Property of P-Methyoxyphenol carbanilate

Chemical Property:

• Vapor Pressure: 2.34E-05mmHg at 25°C
• Boiling Point: 359.6°Cat760mmHg
• Flash Point: 171.3°C
• PSA: 51.05000
• Density: 1.226g/cm³
• LogP: 3.31970
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 243.08954328
• Heavy Atom Count: 18
• Complexity: 256

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)OC(=O)NC2=CC=CC=C2

Technology Process of P-Methyoxyphenol carbanilate

There total 5 articles about P-Methyoxyphenol carbanilate 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: 85.0%

iodobenzene (591-50-4) + carbon monoxide (201230-82-2) + 4-methoxy-phenol (150-76-5) → 4-methoxyphenyl N-phenylcarbamate (19219-48-8)

Guidance literature:

With sodium azide; In 1,4-dioxane; at 60 ℃; for 12h; under 760.051 Torr;

DOI:10.1002/ejoc.201901140

Reference yield: 85.0%

bromobenzene (108-86-1,52753-63-6) + carbon monoxide (201230-82-2) + 4-methoxy-phenol (150-76-5) → 4-methoxyphenyl N-phenylcarbamate (19219-48-8)

Guidance literature:

With sodium azide; In 1,4-dioxane; at 60 ℃; for 12h; under 760.051 Torr;

DOI:10.1002/ejoc.201901140

Reference yield: 56.0%

phenyl isocyanate (103-71-9) + 4-methoxy-phenol (150-76-5) → 4-methoxyphenyl N-phenylcarbamate (19219-48-8)

Guidance literature:

In dichloromethane; at 20 ℃; for 19h; Cooling with ice;

DOI:10.1248/cpb.c18-00394

upstream raw materials:

4-methoxyphenylchloroformate

aniline

4-methoxy-phenol

bis(diphenyl)urea

Downstream raw materials:

phenyl isocyanate

bis(diphenyl)urea

N-butylbenzamide

4-methoxy-phenol

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