[4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester

Base Information

Chemical Name:[4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester
CAS No.:742102-26-7
Molecular Formula:C15H24N2O2
Molecular Weight:264.368
Hs Code.:
DSSTox Substance ID:DTXSID70468572
Wikidata:Q82295834

Synonyms:742102-26-7;Tert-butyl N-[4-(4-aminophenyl)butyl]carbamate;[4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester;SCHEMBL938186;DTXSID70468572;BBYMVZANGNFNNJ-UHFFFAOYSA-N;Carbamic acid, [4-(4-aminophenyl)butyl]-, 1,1-dimethylethyl ester;tert-Butyl(4-(4-aminophenyl)butyl)carbamate;tert-Butyl (4-(4-aminophenyl)butyl)carbamate;EN300-1726452;Z1508689808;N-[4-(4-aminophenyl)butyl]carbamic acid tert-butyl ester

Suppliers and Price of [4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AK Scientific
[4-(4-Aminophenyl)butyl]carbamicacidtert-butylester
1g
$ 1024.00

Total 1 raw suppliers

Chemical Property of [4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester

Chemical Property:

PSA：67.84000
LogP:3.90180
XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:264.183778013
Heavy Atom Count:19
Complexity:266

Purity/Quality:: [4-(4-Aminophenyl)butyl]carbamicacidtert-butylester ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCCCCC1=CC=C(C=C1)N

Technology Process of [4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester

There total 3 articles about [4-(4-Aminophenyl)butyl]carbamic acid tert-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:

: 742102-25-6
[4-(4-Nitrophenyl)but-3-ynyl]carbamic acid tert-butyl ester

: 742102-26-7
[4-(4-aminophenyl)butyl]carbamic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃; under 2585.74 Torr;
DOI:10.1021/jm051134w

Reference yield:

: 636-98-6
p-nitrobenzene iodide

: 742102-26-7
[4-(4-aminophenyl)butyl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: palladium (II) chloride; triphenylphosphine; diethylamine / copper (I) iodide / 20 °C

2: H₂ / Pd/C / ethanol / 20 °C / 2585.74 Torr

With hydrogen; diethylamine; triphenylphosphine; palladium dichloride; palladium on activated charcoal; copper(l) iodide; In ethanol; 1: Sonogashira coupling;
DOI:10.1021/jm051134w

Reference yield:

: 149990-27-2
tert-butyl but-3-yn-1-ylcarbamate

: 742102-26-7
[4-(4-aminophenyl)butyl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: palladium (II) chloride; triphenylphosphine; diethylamine / copper (I) iodide / 20 °C

2: H₂ / Pd/C / ethanol / 20 °C / 2585.74 Torr

With hydrogen; diethylamine; triphenylphosphine; palladium dichloride; palladium on activated charcoal; copper(l) iodide; In ethanol; 1: Sonogashira coupling;
DOI:10.1021/jm051134w