C₂₄H₃₉N₂O₃PS

Base Information

Chemical Name:C₂₄H₃₉N₂O₃PS
CAS No.:329347-52-6
Molecular Formula:C₂₄H₃₉N₂O₃PS
Molecular Weight:466.625
Hs Code.:

C<sub>24</sub>H<sub>39</sub>N<sub>2</sub>O<sub>3</sub>PS

Synonyms:

Suppliers and Price of C₂₄H₃₉N₂O₃PS

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 C₂₄H₃₉N₂O₃PS

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₄H₃₉N₂O₃PS

There total 7 articles about C₂₄H₃₉N₂O₃PS 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:

: 66081-21-8
2-azidobenzenesulphonamide

: 329347-52-6
C₂₄H₃₉N₂O₃PS

Guidance literature:: Multi-step reaction with 6 steps

1: thionyl chloride; pyridine / CH₂Cl₂ / 4 h / 25 °C

2: CH₂Cl₂ / 18 h / 25 °C

3: toluene

4: tetrahydrofuran / -40 °C

5: trimethyl phosphite; methanol / 60 °C

With pyridine; methanol; thionyl chloride; phosphorous acid trimethyl ester; In tetrahydrofuran; dichloromethane; toluene; 2: Diels-Alder reaction / 3: Staudinger reaction / 6: Dess-Martin oxidation;
DOI:10.1016/S0040-4039(00)01797-4

Reference yield:

: 3306-62-5
2-AMINOBENZENESULFONAMIDE

: 329347-52-6
C₂₄H₃₉N₂O₃PS

Guidance literature:: Multi-step reaction with 7 steps

1.1: aq. HCl; NaNO₂ / 0 °C

1.2: sodium azide; aq. NaOAc

2.1: thionyl chloride; pyridine / CH₂Cl₂ / 4 h / 25 °C

3.1: CH₂Cl₂ / 18 h / 25 °C

4.1: toluene

5.1: tetrahydrofuran / -40 °C

6.1: trimethyl phosphite; methanol / 60 °C

With pyridine; hydrogenchloride; methanol; thionyl chloride; sodium nitrite; phosphorous acid trimethyl ester; In tetrahydrofuran; dichloromethane; toluene; 3.1: Diels-Alder reaction / 4.1: Staudinger reaction / 7.1: Dess-Martin oxidation;
DOI:10.1016/S0040-4039(00)01797-4

Reference yield:

: C₆H₄N₄O₃S₂

: 329347-52-6
C₂₄H₃₉N₂O₃PS

Guidance literature:: Multi-step reaction with 5 steps

1: CH₂Cl₂ / 18 h / 25 °C

2: toluene

3: tetrahydrofuran / -40 °C

4: trimethyl phosphite; methanol / 60 °C

With methanol; phosphorous acid trimethyl ester; In tetrahydrofuran; dichloromethane; toluene; 1: Diels-Alder reaction / 2: Staudinger reaction / 5: Dess-Martin oxidation;
DOI:10.1016/S0040-4039(00)01797-4