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

Encyclopedia

Tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate

Base Information Edit
  • Chemical Name:Tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate
  • CAS No.:149771-44-8
  • Molecular Formula:C11H20 N2 O2
  • Molecular Weight:212.292
  • Hs Code.:2933990090
  • European Community (EC) Number:815-968-7
  • DSSTox Substance ID:DTXSID60577768
  • Nikkaji Number:J1.659.869K
  • Mol file:149771-44-8.mol
Tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate

Synonyms:149771-44-8;tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate;8-Boc-3,8-diaza-bicyclo[3.2.1]octane;8-Boc-3,8-diazabicyclo[3.2.1]octane;C11H20N2O2;3,8-Diazabicyclo[3.2.1]octane-8-carboxylic acid, 1,1-dimethylethyl ester;MFCD17016708;1,1-dimethylethyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate;CYCLOHEXYLANTHRANILATE;8-t-butoxycarbonyl-3,8-diazabicyclo[3.2.1]octane;SCHEMBL178638;DTXSID60577768;HNINFCBLGHCFOJ-UHFFFAOYSA-N;MFCD04115137;AKOS005166981;AB19687;CS-W019596;GS-0910;SB20132;AM803244;SY020355;EN300-90564;A808957;J-519373;8-tert-butoxycarbonyl-3,8-diazabicyclo[3.2.1]octane;8-(tert-butoxycarbonyl)-3,8-diazabicyclo[3.2.1]octane;F2147-1665;Z1083213962;tert-Butyl 3,8-diazabicyclo-[3.2.1]octane-8-carboxylate;3,8-diaza-bicyclo[3,2,1]octane-8-carboxyli acid tert-butyl ester;3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester

Suppliers and Price of Tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate
Supply Marketing:Edit
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
  • 8-Boc-3,8-diaza-bicyclo[3.2.1]octane
  • 25mg
  • $ 355.00
  • TRC
  • tert-Butyl3,8-Diazabicyclo[3.2.1]octane-8-carboxylate
  • 250mg
  • $ 50.00
  • Synthonix
  • 8-Boc-3,8-diaza-bicyclo[3.2.1]octane 95+%
  • 5g
  • $ 170.00
  • Synthonix
  • 8-Boc-3,8-diaza-bicyclo[3.2.1]octane 95+%
  • 1g
  • $ 40.00
  • SynQuest Laboratories
  • 3,8-Diazabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester
  • 250 mg
  • $ 160.00
  • SynQuest Laboratories
  • 3,8-Diazabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester
  • 5 g
  • $ 880.00
  • SynQuest Laboratories
  • 3,8-Diazabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester
  • 1 g
  • $ 320.00
  • Matrix Scientific
  • tert-Butyl 3,8-diazabicyclo-[3.2.1]octane-8-carboxylate 95+%
  • 1g
  • $ 245.00
  • Matrix Scientific
  • tert-Butyl 3,8-diazabicyclo-[3.2.1]octane-8-carboxylate 95+%
  • 5g
  • $ 738.00
  • Matrix Scientific
  • tert-Butyl 3,8-diazabicyclo-[3.2.1]octane-8-carboxylate 95+%
  • 250mg
  • $ 115.00
Total 58 raw suppliers
Chemical Property of Tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate Edit
Chemical Property:
  • Vapor Pressure:0.002mmHg at 25°C 
  • Refractive Index:1.494 
  • Boiling Point:295.4oC at 760mmHg 
  • PKA:9.53±0.20(Predicted) 
  • Flash Point:132.5oC 
  • PSA:41.57000 
  • Density:1.076g/cm3 
  • LogP:1.62440 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C 
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:212.152477885
  • Heavy Atom Count:15
  • Complexity:248
Purity/Quality:

97% *data from raw suppliers

8-Boc-3,8-diaza-bicyclo[3.2.1]octane *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)N1C2CCC1CNC2
  • Uses tert-Butyl 3,8-Diazabicyclo[3.2.1]octane-8-carboxylate is used in preparation of isoquinolinone derivatives and pharmaceutical compounds thereof for prevention or treatment of poly(ADP-ribose)polymerase-1 (PARP-1)-associated diseases.
Technology Process of Tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate

There total 16 articles about Tert-butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate 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 hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm970427p
Guidance literature:
With potassium carbonate; In methanol; water; at 20 ℃; for 16h;
Guidance literature:
With water; 1-dodecylthiol; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
Post RFQ for Price