N-BOC 4-morpholinoaniline

Base Information

Chemical Name:N-BOC 4-morpholinoaniline
CAS No.:564483-40-5
Molecular Formula:C15H22N2O3
Molecular Weight:278.351
Hs Code.:2934999090
DSSTox Substance ID:DTXSID80467359
Nikkaji Number:J1.911.693J
Wikidata:Q82294293

Synonyms:N-BOC 4-morpholinoaniline;564483-40-5;Tert-butyl N-(4-morpholin-4-ylphenyl)carbamate;TERT-BUTYL N-[4-(MORPHOLIN-4-YL)PHENYL]CARBAMATE;tert-Butyl [4-(morpholin-4-yl)phenyl]carbamate;t-butyl 4-morpholinophenylcarbamate;N-BOC4-morpholinoaniline;SCHEMBL8346062;DTXSID80467359;SRMBUHFNPUQJFY-UHFFFAOYSA-N;AKOS014475980;BS-29190;1,1-Dimethylethyl N-[4-(4-morpholinyl)phenyl]carbamate

Suppliers and Price of N-BOC 4-morpholinoaniline

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
N-BOC4-morpholinoaniline 95+%
5g
$ 371.00

Chemenu
N-BOC4-morpholinoaniline 95%
5g
$ 351.00

AK Scientific
N-BOC4-morpholinoaniline
1g
$ 611.00

Total 1 raw suppliers

Chemical Property of N-BOC 4-morpholinoaniline

Chemical Property:

PSA：50.80000
LogP:3.00820
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:278.16304257
Heavy Atom Count:20
Complexity:314

Purity/Quality:: N-BOC4-morpholinoaniline 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)N2CCOCC2

Technology Process of N-BOC 4-morpholinoaniline

There total 3 articles about N-BOC 4-morpholinoaniline 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: 89.0%

: 2524-67-6,86759-37-7
4-morpholino-4-yl-phenylamine

: 24424-99-5
di-tert-butyl dicarbonate

: 564483-40-5
(4-morpholin-4-ylphenyl)carbamic acid tert-butyl ester

Guidance literature:: In dichloromethane; at 20 ℃;

Reference yield: 81.0%

: 110-91-8,99108-56-2
morpholine

: 18437-66-6
N-(t-butoxycarbonyl)-4-chloroaniline

: 564483-40-5
(4-morpholin-4-ylphenyl)carbamic acid tert-butyl ester

Guidance literature:: With tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; sodium t-butanolate; XPhos; In tert-butyl alcohol; at 100 ℃; for 0.5h;
DOI:10.1021/ja035483w

Reference yield: 46.0%

: 110-91-8,99108-56-2
morpholine

: 60144-53-8
N-(tert-butoxycarbonyl)-4-fluoroaniline

: 564483-40-5
(4-morpholin-4-ylphenyl)carbamic acid tert-butyl ester

Guidance literature:: With silver(I) hexafluorophosphate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; C₁₅H₁₅F₂OP; In tetrahydrofuran; at 120 ℃; for 20h; Inert atmosphere; Molecular sieve;
DOI:10.1021/jacs.9b13684