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Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester

Base Information
  • Chemical Name:Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester
  • CAS No.:178394-53-1
  • Molecular Formula:C16H26O2
  • Molecular Weight:250.381
  • Hs Code.:
Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester

Synonyms:Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester

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Chemical Property of Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester
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Technology Process of Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester

There total 1 articles about Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester 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:
Multi-step reaction with 5 steps
1: KMnO4; MgSO4 / acetone / 20 °C
2: 66 percent / oxygen / 1,2-dimethoxy-ethane / 4 h / 20 °C
3: 95 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
4: 8 percent / molecular sieves 4 Angstroem; N-methylmorpholine N-oxide; tetra-n-propylammonium perruthenate / CH2Cl2
5: 94 percent / NaHCO3; m-chloroperbenzoic acid / CH2Cl2 / -78 °C
With potassium permanganate; lithium aluminium tetrahydride; tetrapropylammonium perruthennate; 4 A molecular sieve; oxygen; sodium hydrogencarbonate; magnesium sulfate; 4-methylmorpholine N-oxide; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; acetone; 5: Baeyer-Villiger oxidation;
DOI:10.1080/00397910500377172
Guidance literature:
Multi-step reaction with 5 steps
1.1: 95 percent / potassium hydroxide / methanol / 20 °C
2.1: 85 percent / molecular sieves 4 Angstroem; N-methylmorpholine N-oxide; tetra-n-propylammonium perruthenate / CH2Cl2
3.1: sec-butyllithium / hexane; tetrahydrofuran / 0 - 20 °C
3.2: 93 percent / hexane; tetrahydrofuran / 1 h
4.1: 94 percent / Li; liq. ammonia / tetrahydrofuran / 0.33 h / -78 °C
5.1: 94 percent / pyridinium p-toluenesulfonate / ethanol / 2 h / 20 °C
With potassium hydroxide; tetrapropylammonium perruthennate; 4 A molecular sieve; ammonia; sec.-butyllithium; pyridinium p-toluenesulfonate; lithium; 4-methylmorpholine N-oxide; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane;
DOI:10.1080/00397910500377172
Guidance literature:
Multi-step reaction with 4 steps
1.1: 95 percent / potassium hydroxide / methanol / 20 °C
2.1: 85 percent / molecular sieves 4 Angstroem; N-methylmorpholine N-oxide; tetra-n-propylammonium perruthenate / CH2Cl2
3.1: sec-butyllithium / hexane; tetrahydrofuran / 0 - 20 °C
3.2: 93 percent / hexane; tetrahydrofuran / 1 h
4.1: 94 percent / Li; liq. ammonia / tetrahydrofuran / 0.33 h / -78 °C
With potassium hydroxide; tetrapropylammonium perruthennate; 4 A molecular sieve; ammonia; sec.-butyllithium; lithium; 4-methylmorpholine N-oxide; In tetrahydrofuran; methanol; hexane; dichloromethane;
DOI:10.1080/00397910500377172
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