C₂₆H₃₈N₂O₈

Base Information

Chemical Name:C₂₆H₃₈N₂O₈
CAS No.:485808-73-9
Molecular Formula:C₂₆H₃₈N₂O₈
Molecular Weight:506.596
Hs Code.:

C<sub>26</sub>H<sub>38</sub>N<sub>2</sub>O<sub>8</sub>

Synonyms:C₂₆H₃₈N₂O₈

Suppliers and Price of C₂₆H₃₈N₂O₈

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 0 raw suppliers

Chemical Property of C₂₆H₃₈N₂O₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₆H₃₈N₂O₈

There total 4 articles about C₂₆H₃₈N₂O₈ 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:

: 2480-93-5
Boc-Orn(Z)-OH

: 485808-73-9
C₂₆H₃₈N₂O₈

Guidance literature:: Multi-step reaction with 6 steps

1.1: isobutyl chloroformate; triethylamine / tetrahydrofuran / -15 °C

1.2: 95 percent / NaBH₄ / H₂O

2.1: 97 percent / imidazole / dimethylformamide

3.1: 97 percent / DMAP / acetonitrile

4.1: 99 percent / TBAF / tetrahydrofuran

5.1: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -65 °C

6.1: 92 percent / K₂CO₃; 18-crown-6 / toluene; acetonitrile / -15 °C

With 1H-imidazole; dmap; oxalyl dichloride; 18-crown-6 ether; tetrabutyl ammonium fluoride; potassium carbonate; dimethyl sulfoxide; triethylamine; isobutyl chloroformate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile; 5.1: Swern oxidation / 6.1: Horner-Emmons olefination;
DOI:10.1021/ol0269852

Reference yield:

: 485808-70-6
[4-tert-butoxycarbonylamino-5-(tert-butyl-dimethyl-silanyloxy)-pentyl]-carbamic acid benzyl ester

: 485808-73-9
C₂₆H₃₈N₂O₈

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / DMAP / acetonitrile

2: 99 percent / TBAF / tetrahydrofuran

3: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -65 °C

4: 92 percent / K₂CO₃; 18-crown-6 / toluene; acetonitrile / -15 °C

With dmap; oxalyl dichloride; 18-crown-6 ether; tetrabutyl ammonium fluoride; potassium carbonate; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; toluene; acetonitrile; 3: Swern oxidation / 4: Horner-Emmons olefination;
DOI:10.1021/ol0269852

Reference yield:

: 485808-72-8
C₂₃H₃₆N₂O₇

: 485808-73-9
C₂₆H₃₈N₂O₈

Guidance literature:: Multi-step reaction with 2 steps

1: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -65 °C

2: 92 percent / K₂CO₃; 18-crown-6 / toluene; acetonitrile / -15 °C

With oxalyl dichloride; 18-crown-6 ether; potassium carbonate; dimethyl sulfoxide; triethylamine; In dichloromethane; toluene; acetonitrile; 1: Swern oxidation / 2: Horner-Emmons olefination;
DOI:10.1021/ol0269852