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C30H49NO7

Base Information
  • Chemical Name:C30H49NO7
  • CAS No.:1302981-87-8
  • Molecular Formula:C30H49NO7
  • Molecular Weight:535.722
  • Hs Code.:
C<sub>30</sub>H<sub>49</sub>NO<sub>7</sub>

Synonyms:C30H49NO7

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Chemical Property of C30H49NO7
Chemical Property:
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Technology Process of C30H49NO7

There total 13 articles about C30H49NO7 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:
Guidance literature:
With potassium fluoride; In isopropyl alcohol; at 22 ℃;
DOI:10.1016/j.tetlet.2010.11.012
Guidance literature:
Multi-step reaction with 13 steps
1.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane
2.1: chloro-trimethyl-silane; lithium diisopropyl amide / tetrahydrofuran
2.2: 12 h / Reflux
4.1: tetrabutyl ammonium fluoride
5.1: pyridine
6.1: potassium tert-butylate
7.1: lithium aluminium tetrahydride / diethyl ether / -20 °C
8.1: sodium hydrogencarbonate; Dess-Martin periodane
9.1: tetrahydrofuran / -78 °C
10.1: dmap / dichloromethane
11.1: diisobutylaluminium hydride / -78 °C
12.1: sodium hydrogencarbonate; Dess-Martin periodane
13.1: potassium fluoride / isopropyl alcohol / 22 °C
With pyridine; dmap; potassium fluoride; lithium aluminium tetrahydride; chloro-trimethyl-silane; potassium tert-butylate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; sodium hydrogencarbonate; Dess-Martin periodane; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane; isopropyl alcohol; 2.1: Claisen rearrangement / 2.2: Claisen rearrangement / 8.1: Dess-Martin oxidation / 9.1: Aldol condensation / 12.1: Dess-Martin oxidation / 13.1: Henry reaction;
DOI:10.1016/j.tetlet.2010.11.012
Guidance literature:
Multi-step reaction with 12 steps
1.1: chloro-trimethyl-silane; lithium diisopropyl amide / tetrahydrofuran
1.2: 12 h / Reflux
3.1: tetrabutyl ammonium fluoride
4.1: pyridine
5.1: potassium tert-butylate
6.1: lithium aluminium tetrahydride / diethyl ether / -20 °C
7.1: sodium hydrogencarbonate; Dess-Martin periodane
8.1: tetrahydrofuran / -78 °C
9.1: dmap / dichloromethane
10.1: diisobutylaluminium hydride / -78 °C
11.1: sodium hydrogencarbonate; Dess-Martin periodane
12.1: potassium fluoride / isopropyl alcohol / 22 °C
With pyridine; dmap; potassium fluoride; lithium aluminium tetrahydride; chloro-trimethyl-silane; potassium tert-butylate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; sodium hydrogencarbonate; Dess-Martin periodane; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane; isopropyl alcohol; 1.1: Claisen rearrangement / 1.2: Claisen rearrangement / 7.1: Dess-Martin oxidation / 8.1: Aldol condensation / 11.1: Dess-Martin oxidation / 12.1: Henry reaction;
DOI:10.1016/j.tetlet.2010.11.012
upstream raw materials:

C31H40O4Si

C41H58O5Si

C42H60O5Si

C26H40O4

Downstream raw materials:

C30H47NO6

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