C₄₁H₇₃NO₈S

Base Information

Chemical Name:C₄₁H₇₃NO₈S
CAS No.:1431220-28-8
Molecular Formula:C₄₁H₇₃NO₈S
Molecular Weight:740.099
Hs Code.:

C<sub>41</sub>H<sub>73</sub>NO<sub>8</sub>S

Synonyms:C₄₁H₇₃NO₈S

Suppliers and Price of C₄₁H₇₃NO₈S

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 C₄₁H₇₃NO₈S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₁H₇₃NO₈S

There total 18 articles about C₄₁H₇₃NO₈S 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: 100.0%

: 1431220-34-6
C₆₂H₉₁NO₈S

: 1431220-28-8
C₄₁H₇₃NO₈S

Guidance literature:: With ammonia; sodium; In tetrahydrofuran; at -78 ℃; for 2h; Inert atmosphere;
DOI:10.3998/ark.5550190.0014.224

Reference yield:

: 88303-25-7
tetradecylmagnesium bromide

: 1431220-28-8
C₄₁H₇₃NO₈S

Guidance literature:: Multi-step reaction with 12 steps

1.1: tetrahydrofuran

2.1: pyridine

3.1: toluene-4-sulfonic acid / methanol; dichloromethane

4.1: sodium azide / N,N-dimethyl-formamide / Heating

5.1: toluene-4-sulfonic acid

6.1: pyridine

7.1: lithium iodide / N,N-dimethyl-formamide

8.1: sodium hydrogencarbonate; tetra(n-butyl)ammonium hydrogensulfate / ethyl acetate

9.1: triphenylphosphine / tetrahydrofuran / 2 h / 20 °C

9.2: Staudinger Azide Reduction / 2 h

10.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

11.1: hydrogenchloride / methanol; dichloromethane; 1,4-dioxane / 2.5 h / 20 °C

12.1: sodium; ammonia / tetrahydrofuran / 2 h / -78 °C / Inert atmosphere

With pyridine; hydrogenchloride; sodium azide; ammonia; tetra(n-butyl)ammonium hydrogensulfate; sodium; sodium hydrogencarbonate; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; lithium iodide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; 1.1: |Grignard Reaction / 9.1: |Staudinger Azide Reduction / 12.1: |Birch Reduction;
DOI:10.3998/ark.5550190.0014.224

Reference yield:

: 160280-65-9
(2R,3R,4R)-1,3,4-trihydroxyoctadecan-2-yl methanesulfonate

: 1431220-28-8
C₄₁H₇₃NO₈S

Guidance literature:: Multi-step reaction with 10 steps

1.1: sodium azide / N,N-dimethyl-formamide / Heating

2.1: toluene-4-sulfonic acid

3.1: toluene-4-sulfonic acid / methanol; dichloromethane

4.1: pyridine

5.1: lithium iodide / N,N-dimethyl-formamide

6.1: sodium hydrogencarbonate; tetra(n-butyl)ammonium hydrogensulfate / ethyl acetate

7.1: triphenylphosphine / tetrahydrofuran / 2 h / 20 °C

7.2: Staudinger Azide Reduction / 2 h

8.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

9.1: hydrogenchloride / methanol; dichloromethane; 1,4-dioxane / 2.5 h / 20 °C

10.1: sodium; ammonia / tetrahydrofuran / 2 h / -78 °C / Inert atmosphere

With pyridine; hydrogenchloride; sodium azide; ammonia; tetra(n-butyl)ammonium hydrogensulfate; sodium; sodium hydrogencarbonate; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; lithium iodide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; 7.1: |Staudinger Azide Reduction / 10.1: |Birch Reduction;
DOI:10.3998/ark.5550190.0014.224