Z-8-aMino-3,6-dioxaoctanoic acid

Base Information

Chemical Name:Z-8-aMino-3,6-dioxaoctanoic acid
CAS No.:1345337-22-5
Molecular Formula:C₂₁H₄₃NO₁₀
Molecular Weight:469.573
Hs Code.:
Mol file:1345337-22-5.mol

Synonyms:

Suppliers and Price of Z-8-aMino-3,6-dioxaoctanoic acid

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

TRC
N-Boc-PEG8-alcohol
10mg
$ 45.00

purepeg
BocNH-PEG8-OH min.97%
250 mg
$ 250.00

chempep
Z-NH-PEG2-CH2COOH >=95%
5g
$ 558.00

chempep
Z-NH-PEG2-CH2COOH >=95%
1g
$ 250.00

BroadPharm
N-Boc-PEG8-alcohol 98%
500 MG
$ 360.00

BroadPharm
N-Boc-PEG8-alcohol 98%
1 G
$ 500.00

BroadPharm
N-Boc-PEG8-alcohol 98%
5 G
$ 1500.00

AK Scientific
N-Boc-PEG8-alcohol
1g
$ 1072.00

Activate Scientific
BocNH-PEG8-OH 95+%
1 g
$ 634.00

Acrotein
BocNH-PEG8-OH 97%
1g
$ 495.00

Total 12 raw suppliers

Chemical Property of Z-8-aMino-3,6-dioxaoctanoic acid

Chemical Property:

Boiling Point:553.7±50.0 °C(Predicted)
PKA:12.23±0.46(Predicted)
Density:1.093±0.06 g/cm3(Predicted)

Purity/Quality:

98%,99%, ^*data from raw suppliers

N-Boc-PEG8-alcohol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description N-Boc-PEG8-alcohol is a PEG linker containing a hydroxyl group and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Technology Process of Z-8-aMino-3,6-dioxaoctanoic acid

There total 1 articles about Z-8-aMino-3,6-dioxaoctanoic acid 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

: 352439-37-3
23-amino-3 ,6,9,12,15,18,21-heptaoxatricosan-1-ol

: 1345337-22-5
C₂₁H₄₃NO₁₀

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In chloroform; at 20 ℃; for 1h;
DOI:10.1039/c1cc14728e

Reference yield:

: 1345337-22-5
C₂₁H₄₃NO₁₀

: 1358996-28-7
C₄₂H₇₅N₃O₁₃

Guidance literature:: Multi-step reaction with 2 steps

1: chloroform / 2 h

2: N-ethyl-N,N-diisopropylamine / chloroform / Reflux

With N-ethyl-N,N-diisopropylamine; In chloroform;
DOI:10.1039/c1cc14728e