tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate

Base Information

Chemical Name:tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate
CAS No.:275385-03-0
Molecular Formula:C₁₃H₂₇NO₆
Molecular Weight:293.36
Hs Code.:

Synonyms:

Suppliers and Price of tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate

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

BroadPharm
N-Boc-N-bis(PEG1-OH) 98%
1 G
$ 980.00

BroadPharm
N-Boc-N-bis(PEG1-OH) 98%
250 MG
$ 380.00

Total 7 raw suppliers

Chemical Property of tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate

Chemical Property:

Purity/Quality:

>98.0% ^*data from raw suppliers

N-Boc-N-bis(PEG1-OH) 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description N-Boc-N-bis(PEG1-OH) is a small PEG linker compound with two terminal hydroxy groups and a Boc protected amino group. The hydroxy groups enable further derivatization or replacement with other reactive functional groups. Boc can be deprotected under acidic conditions.

Technology Process of tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate

There total 1 articles about tert-butyl bis(2-(2-hydroxyethoxy)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:

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

: 54384-47-3
2,2'-((azanediylbis(ethane-2,1-diyl))bis(oxy))diethanol

: 275385-03-0
tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 18h;

Reference yield:

: 275385-03-0
tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate

: bis(2-(2-p-toluenesulfonylethoxy)ethyl)amine

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 18 h / 20 °C

2: trifluoroacetic acid / dichloromethane / 2 h / 0 - 20 °C

With triethylamine; trifluoroacetic acid; In dichloromethane;

Reference yield:

: 275385-03-0
tert-butyl bis(2-(2-hydroxyethoxy)ethyl)carbamate

: 4-(bis(2-(2-(p-toluenesulfonyloxy)ethoxy)ethyl)amino)-4-oxobutanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 18 h / 20 °C

2: trifluoroacetic acid / dichloromethane / 2 h / 0 - 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C

With triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane;