3-[3-(Trifluoromethyl)phenyl]octahydropyrido[2,1-c][1,4]oxazin-3-ol

Base Information

• Chemical Name: 3-[3-(Trifluoromethyl)phenyl]octahydropyrido[2,1-c][1,4]oxazin-3-ol
• CAS No.: 63068-72-4
• Molecular Formula: C₁₅H₁₈F₃NO₂
• Molecular Weight: 301.309
• ChEMBL ID: CHEMBL3303439
• DSSTox Substance ID: DTXSID20497857

Synonyms:63068-72-4;CHEMBL3303439;DTXSID20497857;3-[3-(Trifluoromethyl)phenyl]octahydropyrido[2,1-c][1,4]oxazin-3-ol

Chemical Property of 3-[3-(Trifluoromethyl)phenyl]octahydropyrido[2,1-c][1,4]oxazin-3-ol

Chemical Property:

• PSA: 32.70000
• LogP: 2.67310
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 301.12896330
• Heavy Atom Count: 21
• Complexity: 376

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN2CC(OCC2C1)(C3=CC(=CC=C3)C(F)(F)F)O

Technology Process of 3-[3-(Trifluoromethyl)phenyl]octahydropyrido[2,1-c][1,4]oxazin-3-ol

There total 1 articles about 3-[3-(Trifluoromethyl)phenyl]octahydropyrido[2,1-c][1,4]oxazin-3-ol 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:

→ 3-(3-trifluoromethyl-phenyl)-(9ar)-octahydro-pyrido[2,1-c][1,4]oxazin-3t-ol (63068-72-4)

Guidance literature:

entspr. 2-Bromacetophenon, 2-Piperidinmethanol;

DOI:10.1021/jm00203a010

Reference yield:

3-(3-trifluoromethyl-phenyl)-(9ar)-octahydro-pyrido[2,1-c][1,4]oxazin-3t-ol (63068-72-4) → 3c-(3-trifluoromethyl-phenyl)-(9ar)-octahydro-pyrido[2,1-c][1,4]oxazine

Guidance literature:

Multistep reaction; (i) H₂, Pd(OH)2-C, aq. H₂SO₄, (ii) aq. HBr;

DOI:10.1021/jm00203a010

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