Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

[4-({6-[Allyl(methyl)amino]hexyl}oxy)-2-fluorophenyl](4-bromophenyl)methanone

Base Information
  • Chemical Name:[4-({6-[Allyl(methyl)amino]hexyl}oxy)-2-fluorophenyl](4-bromophenyl)methanone
  • CAS No.:161582-11-2
  • Molecular Formula:C23H27 Br F N O2
  • Molecular Weight:448.375
  • Hs Code.:
  • UNII:YDR69X9Q9M
  • DSSTox Substance ID:DTXSID90870077
  • Nikkaji Number:J825.077D
  • Wikidata:Q27088590
  • Pharos Ligand ID:3A6LWHZMB9PH
  • Metabolomics Workbench ID:146628
  • ChEMBL ID:CHEMBL304858
  • Mol file:161582-11-2.mol
[4-({6-[Allyl(methyl)amino]hexyl}oxy)-2-fluorophenyl](4-bromophenyl)methanone

Synonyms:(4'-(6-allylmethylaminohexyloxy)-2'-fluorophenyl)-4-(4-bromophenyl)methanone fumarate;Ro 48-8071;Ro 48-8071hydrochloride;Ro-48-8071

Suppliers and Price of [4-({6-[Allyl(methyl)amino]hexyl}oxy)-2-fluorophenyl](4-bromophenyl)methanone
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
  • Usbiological
  • Ro 48-8071
  • 5mg
  • $ 326.00
  • TRC
  • Ro48-8071
  • 10mg
  • $ 100.00
  • DC Chemicals
  • Ro48-8071 >98%
  • 100 mg
  • $ 352.00
  • DC Chemicals
  • Ro48-8071 >98%
  • 10 mg
  • $ 56.00
  • Cayman Chemical
  • Ro 48-8071 ≥95%
  • 50mg
  • $ 264.00
  • Cayman Chemical
  • Ro 48-8071 ≥95%
  • 10mg
  • $ 63.00
  • Cayman Chemical
  • Ro 48-8071 ≥95%
  • 100mg
  • $ 462.00
  • Cayman Chemical
  • Ro 48-8071 ≥95%
  • 5mg
  • $ 33.00
  • Biorbyt Ltd
  • Ro 48-8071
  • 100 mg
  • $ 544.00
  • Biorbyt Ltd
  • Ro 48-8071
  • 50 mg
  • $ 430.10
Total 9 raw suppliers
Chemical Property of [4-({6-[Allyl(methyl)amino]hexyl}oxy)-2-fluorophenyl](4-bromophenyl)methanone
Chemical Property:
  • Vapor Pressure:5.02E-11mmHg at 25°C 
  • Boiling Point:522.8°Cat760mmHg 
  • PKA:8.88±0.50(Predicted) 
  • Flash Point:270°C 
  • PSA:29.54000 
  • Density:1.235g/cm3 
  • LogP:5.87620 
  • Storage Temp.:2-8°C 
  • XLogP3:6.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:12
  • Exact Mass:447.12092
  • Heavy Atom Count:28
  • Complexity:468
Purity/Quality:

≥95% *data from raw suppliers

Ro 48-8071 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN(CCCCCCOC1=CC(=C(C=C1)C(=O)C2=CC=C(C=C2)Br)F)CC=C
  • Description Oxidosqualene cyclase (OSC) is a microsomal enzyme that catalyzes the cyclization of monooxidosqualene to lanosterol in the cholesterol synthetic pathway. Ro 48-8071 is an inhibitor of oxidosqualene cyclase (OSC) that has low-density lipoprotein (LDL) cholesterol lowering activity similar to the 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) inhibitor simvastatin. It inhibits OSC from human liver microsomes and HepG2 cells with IC50 values of approximately 6.5 nM and 1.5 nM, respectively. Ro 48-8071 lowered LDL cholesterol ~40% in hamsters at a dose of 150 μg/kg without affecting high-density lipoprotein levels and with no sign of liver toxicity. Ro 48-8071 increases cytochrome P3A mRNA and protein levels in primary rat and murine hepatocyte cultures with a maximal effect at 30 μM.
  • Uses Ro 48-8071 is an inhibitor of oxidosqualene cyclase.
Technology Process of [4-({6-[Allyl(methyl)amino]hexyl}oxy)-2-fluorophenyl](4-bromophenyl)methanone

There total 7 articles about [4-({6-[Allyl(methyl)amino]hexyl}oxy)-2-fluorophenyl](4-bromophenyl)methanone 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 4 steps
1: aluminum (III) chloride / nitrobenzene / 8 - 20 °C
2: hydrogen bromide; water / acetic acid / 8 h / 125 °C
3: potassium carbonate / acetone / 5 h / 75 °C
4: N,N-dimethyl acetamide / 27 h / 0 - 20 °C
With aluminum (III) chloride; water; hydrogen bromide; potassium carbonate; In N,N-dimethyl acetamide; acetic acid; nitrobenzene; acetone;
Guidance literature:
Multi-step reaction with 2 steps
1: potassium carbonate / acetone / 5 h / 75 °C
2: N,N-dimethyl acetamide / 27 h / 0 - 20 °C
With potassium carbonate; In N,N-dimethyl acetamide; acetone;
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 161582-11-2