Methyl (4-butanamido-3-methoxyphenyl)carbamate

Base Information

Chemical Name:Methyl (4-butanamido-3-methoxyphenyl)carbamate
CAS No.:88149-78-4
Molecular Formula:C13H18N2O4
Molecular Weight:266.297
Hs Code.:
DSSTox Substance ID:DTXSID90552225
Wikidata:Q82432324

Synonyms:88149-78-4;Methyl (4-butanamido-3-methoxyphenyl)carbamate;DTXSID90552225

Suppliers and Price of Methyl (4-butanamido-3-methoxyphenyl)carbamate

Supply Marketing:

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

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Chemical Property of Methyl (4-butanamido-3-methoxyphenyl)carbamate

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:266.12665706
Heavy Atom Count:19
Complexity:309

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(=O)NC1=C(C=C(C=C1)NC(=O)OC)OC

Technology Process of Methyl (4-butanamido-3-methoxyphenyl)carbamate

There total 1 articles about Methyl (4-butanamido-3-methoxyphenyl)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: 91.0%

: 59988-64-6
N-(4-amino-2-methoxyphenyl)butanamide

: 79-22-1
methyl chloroformate

: 88149-78-4
methyl N-<4-(butyramido)-3-methoxyphenyl>carbamate

Guidance literature:: With pyridine; at 20 ℃; for 0.166667h;
DOI:10.1021/jm00392a009

Reference yield:

: 88149-78-4
methyl N-<4-(butyramido)-3-methoxyphenyl>carbamate

: 108835-50-3
[4-(Acridin-9-ylamino)-3-methoxy-phenyl]-carbamic acid methyl ester; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 2 N ethanolic HCl / 1 h / Heating

2: methanol / 0.17 h / Heating

With hydrogenchloride; In methanol;
DOI:10.1021/jm00392a009