2H-Benzo(a)quinolizin-2-ol, 2-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-3-(2-methylpropyl)-

Base Information

• Chemical Name: 2H-Benzo(a)quinolizin-2-ol, 2-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-3-(2-methylpropyl)-
• CAS No.: 303-75-3
• Molecular Formula: C₂₁H₃₃NO₃
• Molecular Weight: 347.498
• European Community (EC) Number: 684-163-9
• UNII: H2S3M5M720
• DSSTox Substance ID: DTXSID90952665
• Nikkaji Number: J11.606H
• Wikidata: Q27279565
• Pharos Ligand ID: 69GNB67YWUPY
• ChEMBL ID: CHEMBL213814
• Mol file: 303-75-3.mol

Synonyms:2H-Benzo(a)quinolizin-2-ol, 2-Ethyl-1,3,4,6,7,11b-hexahydro-3-isobutyl-9,10-dimethoxy-;Ro 4-1284;Ro 41284;Ro4-1284

Chemical Property of 2H-Benzo(a)quinolizin-2-ol, 2-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-3-(2-methylpropyl)-

Chemical Property:

• Vapor Pressure: 1.03E-09mmHg at 25°C
• Boiling Point: 472°C at 760 mmHg
• Flash Point: 239.3°C
• PSA: 41.93000
• Density: 1.1g/cm³
• LogP: 3.74800
• Storage Temp.: 2-8°C
• XLogP3: 3.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 347.24604391
• Heavy Atom Count: 25
• Complexity: 443

Purity/Quality:

99% ^*data from raw suppliers

Ro 4-1284 ^*data from reagent suppliers

Safty Information:

• Pictogram(s): A poison.
• Hazard Codes: N
• Statements: 50/53
• Safety Statements: 60-61

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1(CC2C3=CC(=C(C=C3CCN2CC1CC(C)C)OC)OC)O
• Uses: Ro 4-1284 prevents the thermogenic effects of MDMA, causing a transient decrease in body temperature; P-glycoprotein (P-GP) and brain vesicular monoamine transporter (VMAT2) inhibitor.

Technology Process of 2H-Benzo(a)quinolizin-2-ol, 2-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-3-(2-methylpropyl)-

There total 1 articles about 2H-Benzo(a)quinolizin-2-ol, 2-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-3-(2-methylpropyl)- 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:

→ Ro 4-1284 (303-75-3)

Guidance literature:

Aethinylcarbinol α-Vb, H2;