tert-Butyl (4-benzoylphenyl)carbamate

Base Information

Chemical Name:tert-Butyl (4-benzoylphenyl)carbamate
CAS No.:232597-43-2
Molecular Formula:C18H19NO3
Molecular Weight:297.354
Hs Code.:2924299090
DSSTox Substance ID:DTXSID70697744
Wikidata:Q82627746
Mol file:232597-43-2.mol

Synonyms:tert-Butyl (4-benzoylphenyl)carbamate;232597-43-2;tert-butyl N-(4-benzoylphenyl)carbamate;Carbamic acid, N-(4-benzoylphenyl)-, 1,1-dimethylethyl ester;TERT-BUTYL 4-BENZOYLPHENYLCARBAMATE;tert-Butyl(4-benzoylphenyl)carbamate;SCHEMBL11947174;DTXSID70697744;tert-butyl?4-benzoylphenylcarbamate;AC-9406;FT-0705374;EN300-6249814;A849978

Suppliers and Price of tert-Butyl (4-benzoylphenyl)carbamate

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

Crysdot
tert-Butyl(4-benzoylphenyl)carbamate 95+%
1g
$ 668.00

American Custom Chemicals Corporation
TERT-BUTYL-(4-BENZOYLPHENYL)CARBAMATE 95.00%
5MG
$ 497.59

Alichem
tert-Butyl(4-benzoylphenyl)carbamate
1g
$ 554.88

Total 10 raw suppliers

Chemical Property of tert-Butyl (4-benzoylphenyl)carbamate

Chemical Property:

PSA：55.40000
LogP:4.33760
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:297.13649347
Heavy Atom Count:22
Complexity:386

Purity/Quality:

97% ^*data from raw suppliers

tert-Butyl(4-benzoylphenyl)carbamate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC1=CC=C(C=C1)C(=O)C2=CC=CC=C2

Technology Process of tert-Butyl (4-benzoylphenyl)carbamate

There total 6 articles about tert-Butyl (4-benzoylphenyl)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: 90.0%

: 4248-19-5
tert-butyl carbazate

: 90-90-4
(4-bromophenyl)(phenyl)methanone

: 232597-43-2
N-(tert-Butoxycarbonyl)-4-benzoylaniline

Guidance literature:: With palladium diacetate; caesium carbonate; XPhos; In 1,4-dioxane; at 100 ℃; for 1.5h;
DOI:10.1016/j.tetlet.2010.06.083

Reference yield: 85.0%

: tert-butyl (4-(phenyl(tosyl)carbamoyl)phenyl)carbamate

: 98-80-6
phenylboronic acid

: 232597-43-2
N-(tert-Butoxycarbonyl)-4-benzoylaniline

Guidance literature:: With (bis(tricyclohexyl)phosphine)palladium(II) dichloride; potassium carbonate; tricyclohexylphosphine; In 1,4-dioxane; at 110 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1039/c5cc00430f

Reference yield: 82.0%

: tert-butyl (4-((3,5-bis(trifluoromethyl)phenyl) (tosyl)carbamoyl)phenyl)carbamate

: 143-66-8
sodium tetraphenyl borate

: 232597-43-2
N-(tert-Butoxycarbonyl)-4-benzoylaniline

Guidance literature:: With (bis(tricyclohexyl)phosphine)palladium(II) dichloride; potassium carbonate; tricyclohexylphosphine; In 1,4-dioxane; at 110 ℃; for 10h; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.jorganchem.2015.07.009