tert-butyl (23-azido-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate

Base Information

Chemical Name:tert-butyl (23-azido-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate
CAS No.:206265-96-5
Molecular Formula:C₂₁H₄₂N₄O₉
Molecular Weight:494.586
Hs Code.:

Synonyms:

Suppliers and Price of tert-butyl (23-azido-3,6,9,12,15,18,21-heptaoxatricosyl)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
t-boc-N-amido-PEG7-azide 98%
100 MG
$ 190.00

BroadPharm
t-boc-N-amido-PEG7-azide 98%
500 MG
$ 390.00

BroadPharm
t-boc-N-amido-PEG7-azide 98%
1 G
$ 670.00

Activate Scientific
BocNH-PEG7-CH2CH2N3 95+%
1 g
$ 588.00

Acrotein
BocNH-PEG7-CH2CH2N3 95%
1g
$ 495.00

Acrotein
BocNH-PEG7-CH2CH2N3 95%
0.5g
$ 330.00

Acrotein
BocNH-PEG7-CH2CH2N3 95%
0.25g
$ 220.00

Total 6 raw suppliers

Chemical Property of tert-butyl (23-azido-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

t-boc-N-amido-PEG7-azide 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description t-boc-N-amido-PEG7-azide is a PEG molecule with an azide(N3) group and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group is reactive with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Technology Process of tert-butyl (23-azido-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate

There total 1 articles about tert-butyl (23-azido-3,6,9,12,15,18,21-heptaoxatricosyl)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: