tert-Butyl [2-(2-bromophenoxy)ethyl]carbamate

Base Information

Chemical Name:tert-Butyl [2-(2-bromophenoxy)ethyl]carbamate
CAS No.:1204333-53-8
Molecular Formula:C₁₃H₁₈BrNO₃
Molecular Weight:316.195
Hs Code.:
DSSTox Substance ID:DTXSID10703914
Wikidata:Q82636170

Synonyms:tert-butyl N-[2-(2-bromophenoxy)ethyl]carbamate;1204333-53-8;tert-Butyl [2-(2-bromophenoxy)ethyl]carbamate;DTXSID10703914;BS-35298;tert-butylN-[2-(2-bromophenoxy)ethyl]carbamate;EN300-7385537

Suppliers and Price of tert-Butyl [2-(2-bromophenoxy)ethyl]carbamate

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of tert-Butyl [2-(2-bromophenoxy)ethyl]carbamate

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:315.04701
Heavy Atom Count:18
Complexity:266

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCCOC1=CC=CC=C1Br

Technology Process of tert-Butyl [2-(2-bromophenoxy)ethyl]carbamate

There total 3 articles about tert-Butyl [2-(2-bromophenoxy)ethyl]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: 99.0%

: 459817-82-4
2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester

: 95-56-7
2-hydroxybromobenzene

: 1204333-53-8
C₁₃H₁₈BrNO₃

Guidance literature:: 2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester; 2-hydroxybromobenzene; With sodium hydride; In N,N-dimethyl-formamide;

With hydrogenchloride; In water; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2013.04.090

Reference yield:

: 95-56-7
2-hydroxybromobenzene

: 158690-56-3
2-(tert-butoxycarbonylamino)ethyl-4-methylbenzenesulfonate

: 1204333-53-8
C₁₃H₁₈BrNO₃

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 60 ℃;
DOI:10.1021/acs.jcim.9b00802

Reference yield:

: 26690-80-2
2-(N-tert-butoxycarbonylamino)ethanol

: 1204333-53-8
C₁₃H₁₈BrNO₃

Guidance literature:: Multi-step reaction with 2 steps

1: sodium periodate

2: sodium iodide / N,N-dimethyl-formamide

With sodium periodate; sodium iodide; In N,N-dimethyl-formamide;
DOI:10.1039/c5ra18897k