[N-(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene

Base Information

Chemical Name:[N-(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene
CAS No.:136247-90-0
Molecular Formula:C₁₃H₁₉NO₄
Molecular Weight:253.298
Hs Code.:
DSSTox Substance ID:DTXSID201205944

Synonyms:[N-(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene;ZPIKJPHHBOQGKJ-UHFFFAOYSA-N;DTXSID201205944;136247-90-0;1,1-Dimethylethyl N-[3-(methoxymethoxy)phenyl]carbamate;[N(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene

Suppliers and Price of [N-(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene

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

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Chemical Property of [N-(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:253.13140809
Heavy Atom Count:18
Complexity:262

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of [N-(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene

There total 6 articles about [N-(tert-Butyloxycarbonyl)amino]-3-(methoxymethoxy)benzene 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: 100.0%

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

: 96649-05-7
3-(methoxymethoxy)aniline

: 136247-90-0
tert-butyl (3-(methoxymethoxy)phenyl)carbamate

Guidance literature:: In tetrahydrofuran;

Reference yield:

: 554-84-7
meta-nitrophenol

: 136247-90-0
tert-butyl (3-(methoxymethoxy)phenyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / NaH, Bu₄NI

2: 89 percent / Al-Hg / diethyl ether; H₂O

With aluminium amalgam; tetra-(n-butyl)ammonium iodide; sodium hydride; In diethyl ether; water;
DOI:10.1021/jo971686p

Reference yield:

: 25458-48-4
1-(methoxymethoxy)-3-nitrobenzene

: 136247-90-0
tert-butyl (3-(methoxymethoxy)phenyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / Al-Hg / diethyl ether; H₂O

With aluminium amalgam; In diethyl ether; water;
DOI:10.1021/jo971686p