Benzyl N-(4-aminophenyl)carbamate

Base Information

• Chemical Name: Benzyl N-(4-aminophenyl)carbamate
• CAS No.: 82720-42-1
• Molecular Formula: C14H14N2O2
• Molecular Weight: 242.277
• DSSTox Substance ID: DTXSID40460220
• Nikkaji Number: J1.170.993A
• Mol file: 82720-42-1.mol

Synonyms:82720-42-1;Benzyl N-(4-aminophenyl)carbamate;Benzyl 4-aminophenylcarbamate;Benzyl (4-aminophenyl)carbamate;(4-Amino-phenyl)-carbamic acid benzyl ester;Carbamic acid, (4-aminophenyl)-, phenylmethyl ester;benzyl(4-aminophenyl)carbamate;SCHEMBL1707562;DTXSID40460220;PITLFTKLRFOUEJ-UHFFFAOYSA-N;AMY41859;MFCD06657916;AKOS005835193;AB10139;BS-25923;CS-0132562;EN300-1725883

Chemical Property of Benzyl N-(4-aminophenyl)carbamate

Chemical Property:

• PSA: 64.35000
• LogP: 3.67170
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 242.105527694
• Heavy Atom Count: 18
• Complexity: 257

Purity/Quality:

97% ^*data from raw suppliers

Benzyl(4-aminophenyl)carbamate 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)COC(=O)NC2=CC=C(C=C2)N

Technology Process of Benzyl N-(4-aminophenyl)carbamate

There total 13 articles about Benzyl N-(4-aminophenyl)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: 99.0%

tert-butyl 4-(benzoyloxycarbonylamido)phenylcarbamate (220741-56-0) → (4-Amino-phenyl)-carbamic acid benzyl ester (82720-42-1)

Guidance literature:

In 2,2,2-trifluoroethanol; at 150 ℃; for 2h; microwave irradiation;

DOI:10.1080/00397910802238718

Reference yield: 94.0%

benzyl 4-(nitro)phenylcarbamate (53821-12-8) → (4-Amino-phenyl)-carbamic acid benzyl ester (82720-42-1)

Guidance literature:

With Fe₃O₄Rh; hydrazine hydrate; In ethanol; at 80 ℃; for 5h; Inert atmosphere;

DOI:10.1039/c0cc04816j

Reference yield: 92.0%

4-CbzNHC6H4N3 → (4-Amino-phenyl)-carbamic acid benzyl ester (82720-42-1)

Guidance literature:

With Decaborane; palladium on activated charcoal; In methanol; at 20 ℃; for 5h;

DOI:10.1016/S0040-4039(02)02106-8

upstream raw materials:

benzyl 4-(nitro)phenylcarbamate

benzyl chloroformate

1,4-phenylenediamine

(4-nitroso-phenyl)-carbamic acid benzyl ester

Downstream raw materials:

2-<4-(benzyloxycarboxamido)phenyl>-2-oxo-1,3,2-dioxaphosphorinane

2-<4-(benzyloxycarboxamido)phenyl>-2-oxo-1,3,2-dioxaphospholane

2-<4-(benzyloxycarboxamido)phenyl>-2-oxo-1,3,2-oxazaphosphorinane

N-(bromomethyl)-N'-(benzyloxycarbonyl)-phenylenediamine

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