Carbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl ester

Base Information

Chemical Name:Carbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl ester
CAS No.:260391-75-1
Molecular Formula:C13H19NO4
Molecular Weight:253.298
Hs Code.:
DSSTox Substance ID:DTXSID30442510
Nikkaji Number:J1.276.082E
Wikidata:Q82259819

Synonyms:260391-75-1;Tert-butyl N-(2,4-dimethoxyphenyl)carbamate;(2,4-Dimethoxy-phenyl)-carbamic acid tert-butyl ester;Carbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl ester;Carbamic acid, N-(2,4-dimethoxyphenyl)-, 1,1-dimethylethyl ester;SCHEMBL2589170;DTXSID30442510;UEFXNTMGHGDJRH-UHFFFAOYSA-N;AKOS014476018;SB36249;tert-butyl(2,4-dimethoxyphenyl)carbamate;tert-butyl (2,4-dimethoxyphenyl)carbamate;CS-0340093;FT-0706068;1-(tert-Butoxycarbonylamino)-2,4-dimethoxybenzene;1,1-Dimethylethyl N-(2,4-dimethoxyphenyl)carbamate

Suppliers and Price of Carbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl 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

Total 3 raw suppliers

Chemical Property of Carbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl ester

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:253.13140809
Heavy Atom Count:18
Complexity:275

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Carbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl ester

There total 1 articles about Carbamic acid, (2,4-dimethoxyphenyl)-, 1,1-dimethylethyl 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: 100.0%

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

: 2735-04-8,161687-55-4
2,4-Dimethoxyaniline

: 260391-75-1
N-(tert-butoxycarbonyl)-2,4-dimethoxyamiline

Guidance literature:: copper(II) bis(tetrafluoroborate); at 30 - 33 ℃; for 0.75h;
DOI:10.1016/j.tetlet.2005.12.044

Reference yield: 96.0%

: 67-56-1
methanol

: 260391-75-1
N-(tert-butoxycarbonyl)-2,4-dimethoxyamiline

: N-(tert-butoxycarbonyl)-2-methoxy-p-benzoquinone imine dimethyl acetal

Guidance literature:: With [bis(acetoxy)iodo]benzene; triethylamine; at 20 ℃; for 3h;
DOI:10.1039/c2ob25089f

Reference yield: 71.0%

: 260391-75-1
N-(tert-butoxycarbonyl)-2,4-dimethoxyamiline

: (5-bromo-2,4-dimethoxy-phenyl)-carbamic acid tert-butyl ester

Guidance literature:: With (Bu₄N)₂S₂O₈; lithium bromide; In acetonitrile; at 25 ℃; for 24h;
DOI:10.1016/j.tetlet.2004.04.112 DOI:10.1080/10426500590911395